WO2000047184A1 - Skin sanitizing compositions - Google Patents
Skin sanitizing compositions Download PDFInfo
- Publication number
- WO2000047184A1 WO2000047184A1 PCT/US2000/003511 US0003511W WO0047184A1 WO 2000047184 A1 WO2000047184 A1 WO 2000047184A1 US 0003511 W US0003511 W US 0003511W WO 0047184 A1 WO0047184 A1 WO 0047184A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- skin
- cyclodextrin
- mixtures
- composition according
- agent
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0208—Tissues; Wipes; Patches
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/732—Starch; Amylose; Amylopectin; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/895—Polysiloxanes containing silicon bound to unsaturated aliphatic groups, e.g. vinyl dimethicone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/16—Emollients or protectives, e.g. against radiation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/005—Antimicrobial preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/007—Preparations for dry skin
Definitions
- the present invention relates to compositions and methods of sanitizing and moisturizing skin surfaces.
- an important aspect of the present invention is to provide skin sanitizing compositions providing moisturization and improved skin feel.
- Another aspect of the present invention is to provide skin sanitizing compositions comprising lipophilic moisturizing agents and a degreasing agent.
- One other aspect of the present invention is to provide instant, hand sanitizing compositions comprising lipophilic moisturizing agents and a degreasing agent selected from the group consisting of select silicones, wax materials having a melting point above about 20°C, powders, fluorochemicals and mixtures thereof.
- compositions of the present invention relates to skin sanitizing compositions, comprising: a.) an effective amount of sanitizing agent to kill or reduce the growth of microorganisms, the sanitizing agent comprising from about 40% to about 99% by weight of the composition of alcohol antiseptic; b.) from about 0.1% to about 20% of a lipophilic skin moisturizing agent; c.) an effective amount of a degreasing agent selected from the group consisting of: i.) silicones selected from the group consisting of nonvolatile silicones having a viscosity of at least about 15,000 centipoise, silicone elastomer, silicone elastomer/volatile silicone blends, silicone elastomer/nonvolatile silicone blends, nonvolatile/volatile silicone blends and mixtures thereof; ii.) wax materials soluble in the alcohol antiseptic and having a melting point greater than about 20°C; ii
- the present invention further relate to methods of using the skin sanitizing compositions.
- the skin sanitizing compositions of the present invention can comprise, consist of, or consist essentially of the essential elements and limitations of the invention described herein, as well any of the additional or optional ingredients, components, or limitations described herein.
- alcohol antiseptic means an alcohol (or combination of alcohols) which is effective, at the concentration employed, to kill microorganisms, for example, bacteria, with which it comes in contact.
- compositions of the present invention disinfect the skin area within 30 seconds, preferably 20 seconds without the need for soap and water.
- the skin sanitizing compositions of the present invention including the essential and optional components thereof, are described in detail hereinafter.
- compositions of the present invention also contain from about 40% to about 99%, more preferably from about 50% to about 80%, most preferably from about 55% to about 80% of an alcohol antiseptic or mixtures thereof.
- suitable alcohol antiseptics include, but are not limited to, ethanol, n-propanol and isopropanol and mixtures thereof. Preferred for use herein is ethanol.
- Lipophilic Skin Moisturizing Agent The skin sanitizing compositions of the present invention comprise from about 0.1% to about 20%, preferably from about 1% to about 15%, more preferably from about 2% to about 10%), by weight of the composition, of a lipophilic skin moisturizing agent/emollient.
- the lipophilic skin moisturizing agents suitable for use herein typically have a consistency (k) which ranges from about 0.01 poise to about 10,000 poise, preferably from about 100 poise to about 1000 poise, more preferably from about 200 poise to about 800 poise, and most preferably from about 400 poise to about 500 poise.
- the lipophilic skin moisturizing agent can also desirably be defined in terms of its solubility parameter, as defined by Vaughan in Cosmetics and Toiletries, Vol. 103, p. 47-69, October 1988.
- a lipophilic skin moisturizing agent having a Vaughan solubility Parameter (VSP) of from 5 to 10, preferably from 5.5 to 9 is suitable for use in the moisturizing personal cleansing compositions herein.
- VSP Vaughan solubility Parameter
- the lipophilic skin conditioning agent is selected from the group consisting of hydrocarbon oils and waxes, silicones, fatty acid derivatives, cholesterol, cholesterol derivatives, di- and tri-glycerides, vegetable oils, vegetable oil derivatives, liquid nondigestible oils such as those described in U.S.
- Fatty acids, fatty acid soaps and water soluble polyols are specifically excluded from our definition of a lipophilic skin moisturizing agent.
- Hydrocarbon oils and waxes Some examples are petrolatum, mineral oil micro- crystalline waxes, polyalkenes (e.g. hydrogenated and nonhydrogenated polybutene and polydecene), paraffins, cerasin, ozokerite, polyethylene and perhydrosqualene. Blends of petrolatum and hydrogenated and nonhydrogenated high molecular weight polybutenes wherein the ratio of petrolatum to polybutene ranges from about 90:10 to about 40:60 are also suitable for use as the lipid skin moisturizing agent in the compositions herein.
- Silicone Oils Some examples are dimethicone copolyol, dimethylpolysiloxane, diethylpolysiloxane, high molecular weight dimethicone, mixed C1-C30 alkyl polysiloxane, phenyl dimethicone, dimethiconol, and mixtures thereof. More preferred are non-volatile silicones selected from dimethicone, dimethiconol, mixed C1-C30 alkyl polysiloxane, and mixtures thereof. Nonlimiting examples of silicones useful herein are described in U.S. Patent No. 5,011,681, to Ciotti et al., issued April 30, 1991, which is incorporated by reference.
- Di- and tri-glycerides Some examples are castor oil, soy bean oil, derivatized soybean oils such as maleated soy bean oil, safflower oil, cotton seed oil, corn oil, walnut oil, peanut oil, olive oil, cod liver oil, almond oil, avocado oil, palm oil and sesame oil, vegetable oils and vegetable oil derivatives; coconut oil and derivatized coconut oil, cottonseed oil and derivatized cottonseed oil, jojoba oil, cocoa butter, and the like.
- soy bean oil soy bean oil, derivatized soybean oils such as maleated soy bean oil, safflower oil, cotton seed oil, corn oil, walnut oil, peanut oil, olive oil, cod liver oil, almond oil, avocado oil, palm oil and sesame oil, vegetable oils and vegetable oil derivatives
- coconut oil and derivatized coconut oil, cottonseed oil and derivatized cottonseed oil jojoba oil, cocoa butter, and the like.
- Acetoglyceride esters are used and an example is acetylated monoglycerides.
- Lanolin and its derivatives are preferred and some examples are lanolin, lanolin oil, lanolin wax, lanolin alcohols, lanolin fatty acids, isopropyl lanolate, acetylated lanolin, acetylated lanolin alcohols, lanolin alcohol linoleate, lanolin alcohol riconoleate.
- the lipophilic skin conditioning agent is comprised of lipids selected from the group consisting: petrolatum, blends of petrolatum and high molecular weight polybutene, mineral oil, liquid nondigestible oils (e.g. liquid cottonseed sucrose octaesters) or blends of liquid digestible or nondigestible oils with solid polyol polyesters (e.g.
- sucrose octaesters prepared from C22 fatty acids wherein the ratio of liquid digestible or nondigestible oil to solid polyol polyester ranges from about 96:4 to about 80:20, hydrogenated or nonhydrogenated polybutene, micro- crystalline wax, polyalkene, paraffin, cerasin, ozokerite, polyethylene, perhydrosqualene, dimethicones, alkyl siloxane, polymethylsiloxane, methylphenylpolysiloxane and mixtures thereof.
- the ratio of petrolatum to the other selected lipids is preferably from about 10:1 to about 1 :2, more preferably from about 5 : 1 to about 1 :1.
- Preferred embodiments of the neat cleansing lotions of the aerosol personal cleansing compositions of the present invention are emulsions which comprise a moisturizing phase.
- the moisturizing phase provides the vehicle for delivering the lipophilic skin moisturizing agents to the skin of the user.
- the average droplet size of the moisturizing phase droplets ranges from about 0.005 microns to about 1000 microns, preferably from about 0.1 to about 500 microns, and more preferably from about 0.2 to about 200 microns in diameter. See U.S. Patent Number Re. 34,584, Grote et al, Reissued April 12, 1994, U.S. Patent Number 5,246,694, issued to Birtwistle, on September 21, 1993, and U.S. Patent Number 5,650,84, issued to Gordon et al., on July 22, 1997, all which are herein incorporated by reference.
- the lipophiilic skin moisturizing agent can be thickened using a thickening agent.
- suitable thickening agents for the lipophiilic skin moisturizing agent include polacrylates; fumed silica natural and synthetic waxes, crystalline hydroxy- containing waxes such as trihydroxystearin, alkyl silicone waxes such as behenyl silicone wax; aluminium silicate; lanolin derivatives such as lanesterol; higher fatty alcohols; polyethylenecopolymers; narogel; polyammonium stearate; sucrose esters; hydrophobic clays; petrolatum; hydrotalcites; and mixtures thereof.
- Hydrotalcites are materials of general formula:
- M is a divalent metal ion e.g. Mg ; N is a trivalent metal ion e.g. Al ; X is an exchangeable anion e.g. CO “ , NO " , stearate, cinnimate; m is the number of divalent metal ions; and n is the number of trivalent metal ions.
- Particularly preferred thickening agents for the benefit agent include silica, alkyl silicone waxes, paraffin wax higher fatty alcohols, petroleum jelly and polyethylenecopolymers.
- the thickening agent is preferably from about 4%o to about 25%) by weight based on the level of the lipophilic skin moisturizing agent.
- Degreasing Agent Also essential to the compositions of the present invention are degreasing agents in an effective amount to reduce the greasy feel associated with the lipophilic skin moisturizers.
- degreasing agent as used herein, means an agent which prevents, reduces and/or eliminates the greasy or heavy skin feel typically associated with lipophilic materials.
- Degreasing agents suitable for use in the present invention are selected from the group consisting of select silicones, wax materials soluble in the alcoholic antiseptic and having a melting point greater than about 20°C, powders, fluorochemicals and mixtures thereof, i.) Silicones
- Nonvolatile silicone oils Useful as degreasing agents in the present invention are volatile and non-volatile silicone oils.
- nonvolatile as used herein means that the silicone has a boiling point of at least about 260°C, preferably at least about 275°C, more preferably at least about 300°C. Such materials exhibit very low or no significant vapor pressure at ambient conditions.
- volatile as used herein mean that the silicone has a boiling point of from about 99°C. to about 260°C.
- Volatile silicones suitable for use in the present invention are disclosed in U.S. Patent 4,781,917, issued to Luebbe et al., Nov. 1, 1988 and U.S. Patent 5,759,529 to LeGrow et al, issued June 2, 1998, both of which are herein incorporated by reference in their entirety. Additionally, a description of various volatile silicones materials is found in Todd et al., "Volatile Silicone Fluids for Cosmetics", Cosmetics and Toiletries, 91 :27- 32 (1976). Preferred silicones have surface tensions of less than about 35 dynes, more preferably less than about 30 dynes, most preferably less than about 25 dynes. Particularly preferred volatile silicone oils are selected from the group consisting of cyclic volatile silicones corresponding to the formula:
- n is from about 3 to about 7; and linear volatile silicones corresponding to the formula:
- Linear volatile silicones generally have a viscosity of less than about 5 centistokes at 25. degree. C, whereas the cyclic silicones have viscosities of less than about 10 centistokes at 25. degree. C.
- Highly preferred examples of volatile silicone oils include cyclomethicones of varying viscosities, e.g., Dow Corning 200, Dow Corning 244, Dow Corning 245, Dow Corning 344, and Dow Corning 345, (commercially available from Dow Corning Corp.); SF-1204 and SF-1202 Silicone Fluids (commercially available from G.E.
- volatile silicones comprise at least about or greater than about 3% to about 10%, more preferably from about 4% to about 8%, and most preferably from about 6% to about 8% by weight of the present invention.
- nonvolatile silicones such as fluid silicones and gum silicones.
- the molecular weight and viscosity of the particular selected silicone will determine whether it is a gum or a fluid.
- silicone fluid denotes a silicone with viscosities ranging from about 5 to about 600,000 centistokes, most preferably from about 350 to about 100,000 centistokes, at 25°C.
- silicone gum denotes silicones with mass molecular weights of from about 200,000 to about 1,000,000 and with viscosities greater than about 600,000 centistokes.
- the non-volatile silicones of the present invention preferably have a viscosity of at least about 15,000 centipoise.
- Suitable non-volatile silicones include polysiloxanes and other modified silicones. Polysiloxanes and other modified silicones are described in U.S. Patents 5,650,144 and 5,840,288, both of which are herein incorporated by reference in their entirety. Examples of suitable polysiloxanes and modified silicones include, but are not limited to, polyalkylsiloxanes, polyarylsiloxanes, polyalkylarylsiloxanes, polyestersiloxanes, polyethersiloxane copolymers, polyfluorosiloxanes, polyaminosiloxanes, and mixtures thereof. Preferred non-volatile polysiloxanes are polydimethylsiloxane having viscosities of from about 5 to about 100,000 centistokes at 25°C.
- Silicone fluid and gum mixtures or blends can also be used. Silicone gum and fluid blends are disclosed in U.S. Patent 4,906,459, Cobb et al, issued March 6, 1990; U.S. Patent 4,788,006, Bolich, Jr. et al., issued November 29, 1988; U.S. Patent 4,741,855, Grote et al., issued May 3, 1988; U.S. Patent 4,728,457, Fieler et al., issued March 1, 1988; U.S. Patent 4,704,272, Oh et al., issued November 3, 1987; and U.S. Patent 2,826,551, Geen, issued March 11, 1958; U.S. Patent 5,154,849, Visscher et al., issued October 13, 1992, all of which are herein incorporated by reference in their entirety.
- non-volatile silicones comprise from about 0.01% to about 5%, preferably from about 0.1% to about 2%, more preferably from about 0.1 % to about 1% by weight of the present invention.
- Silicone elastomers are also useful as degreasing agents in the present invention. Suitable silicone elastomers are illustrated in U.S. Patent 5,654,362, herein incorporated by reference in its entirety. Examples of suitable elastomers include, but are not limited to, dimethicone crosspolymer, dimethicone/vinyldimethicone corsspolymer, polysilicone- 11 and mixtures thereof. Such elastomers can be used alone or with volatile or nonvolatile solvents Examples of suitable solvents include, but are not limited to, volatile silicones, volatile alcohols, volatile esters, volatile hydrocarbons, and mixtures thereof. The silicone elastomers are crosslinked and preferably have a weight average molecular weight greater than about 100,000.
- elastomer/solvent blends having an elastomer to solvent ratio of from about 1 :100 to about 1 :1, more preferably from about 1 :30 to about 1 :5.
- the silicone elastomer blend has a viscosity of from about 50,000 centipoise to about 400,000 centipoise, more preferably from about 100,000 centipoise to about 300, 000 centipoise.
- silicone elastomer blends examples include cyclomethicone and dimethicone crosspolymer blend (Dow Corning®9040 silicone elastomer); cyclomethicone and dimethicone/vinyldimethicone cross polymer blend (SFE 839 elastomer dispersion available from GE); octamethylcyclotetrasiloxane and polysilicone- 11 blend (Gransil GCM available from Shin Etsu); and mixtures thereof.
- Preferred herein is the cyclomethicone and dimethicone/vinyldimethicone cross polymer blend.
- the silicone elastomer preferably comprises from about 0.01% to about 5%, preferably from about 0.1% to about 2%.
- silicone elastomer or gum blends preferably comprise from about 0.1% to about 10%), preferably from about 1% to about 10%>, most preferably from about 4% to about 10%) by weight of the composition, ii.) Wax Materials
- Wax materials used herein preferably have melting points of at least about or greater than about 20°C, more preferably at least about or greater than about 25°C, and still more preferably at least about or greater than 32°C, and most preferably at least about or greater than about 35°C.
- the wax materials are preferably soluble in the alcohol antiseptic.
- the phrase "soluble in the alcohol antiseptic," as used herein, means the wax materials is soluble in the alcohol antiseptic, at 25°C, at a concentration of 0.1%, preferably 0.2%, more preferably 0.4% by weight, and most preferably soluble at 1.0% by weight.
- suitable wax materials include, but are not limited to, dimethicone copolyols having a weight average molecular weight greater than about 1000 such as Biowax®. (supplied by Biosil), polyoxyethylene glycols having weight average molecular weight greater than about 500 such as Carbowax (supplied by Union Carbide), and mixtures thereof. Preferred for use herein is Biowax® 754.
- polyoxyethylene glycols having weight average molecular weight greater than about 500, preferably from about 1000 to about 10,000, more preferably from about 1400 to about 6000. Most preferred is PEG-32 (Carbowax 1450).
- the above wax materials preferably comprise from about 0.1% to about 10%, preferably from about 0.1 % to about 5%, most preferably from about 0.4%) to about 2% by weight of the composition, iii.) Powders Also useful as degreasing agents are powders.
- Powder ingredients which may be compounded in the composition of the present invention include inorganic powder such as gums, chalk, Fuller's earth, talc, kaolin, iron oxide, mica, sericite, muscovite, phlogopite, synthetic mica, lepidolite, biotite, lithia mica, vermiculite, magnesium carbonate, calcium carbonate, aluminum silicate, starch, smectite clays, alkyl and/or trialkyl aryl ammonium smectites, chemically modified magnesium aluminum silicate, organically modified montmorillonite clay, hydrated aluminum silicate, fumed silica, aluminum starch octenyl succinate barium silicate, calcium silicate, magnesium silicate, strontium silicate, metal tungstate, magnesium, silica alumina, zeolite, barium sulfate, calcined calcium sulfate (calcined gypsum), calcium phosphate, fluorine apatit
- the powders of the present invention have a particle size such that the average chord length of the powder particles range from about 0.01 microns to about 100 microns, preferably from about 0.1 microns to about 50 microns, more preferably from about 1 micron to about 20 microns.
- the powders of the present invention are spherical or platelet in shape for smooth skin feel.
- the powders can by amorphous or irregular shaped for a draggy skin feel.
- powders preferably comprise from about 0.01% to about 10%, preferably from about 0.1% to about 10%, more preferably from about 0.1%o to about 5%, most preferably from about 0.4%> to about 2% by weight of the composition. iv.) fluorochemicals
- fluorochemicals include fluorotelemers, and perfluoropolyethers, some examples of which are described in Cosmetics & Toiletries, Using Fluorinated Compounds in Topical Preparations, Vol. I l l, pages 47-62, (Oct. 1996) which description is incorporated herein by reference.
- More specific examples of such liquid carriers include, but are not limited to, perfluoropolymethyl isopropyl ethers, perfluoropolypropylethers, acrylamide fluorinated telomer or mixtures thereof.
- Other more specific examples include, but are not limited to, the polyperfluoroisopropyl ethers available from Dupont Performance Chemicals under the trade name Fluortress ® PFPE oils.
- powders When present, powders preferably comprise from about 0.01%> to about 10%, preferably from about 0.1 % to about 2%> by weight of the composition.
- composition comprises three or more lipophilic skin moisturizing agents, two of said lipophilic skin moisturizing agents can also function as a thickening agent or degreasing agent.
- the skin sanitizing compositions of the present invention comprise from about 0% to about 70%), preferably from about 10% to about 50%o, more preferably from about 20% to about 50%, by weight of water.
- cyclodextrin can be added to the compositions of the present invention.
- the term "cyclodextrin” includes any of the known cyclodextrins such as unsubstituted cyclodextrins containing from six to twelve glucose units, especially, alpha-cyclodextrin, beta-cyclodextrin, gamma-cyclodextrin and/or their derivatives and/or mixtures thereof.
- uncomplexed cyclodextrin as used herein means that the cavities within the cyclodextrin in the solution of the present invention should remain essentially unfilled while in solution, in order to allow the cyclodextrin to absorb various odor molecules when the solution is applied to a surface.
- water-soluble, uncomplexed cyclodextrin as used herein means uncomplexed cyclodextrin having a minimum solubility limit of 1%> (1 gram in 100 grams of water).
- Non-derivatised beta-cyclodextrin can be present at a level up to its solubility limit of about 1.85% at room temperature. When beta-cyclodextrin is applied to a wipe substrate, levels higher than its solubility limit can be used.
- Highly water-soluble cyclodextrins are also preferred to be used in the present invention, such as, alpha-cyclodextrin and/or derivatives thereof, gamma-cyclodextrin and/or derivatives thereof, derivatised beta-cyclodextrins, and/or mixtures thereof.
- Highly water-soluble cyclodextrins are those having water solubility of at least about 10 g in 100 ml of water at room temperature, preferably at least about 20 g in 100 ml of water, more preferably at least about 25 g in 100 ml of water at room temperature.
- the derivatives of cyclodextrin consist mainly of molecules wherein some of the OH groups are converted to OR groups.
- Cyclodextrin derivatives include, e.g., those with short chain alkyl groups such as methylated cyclodextrins, and ethylated cyclodextrins, wherein R is a methyl or an ethyl group; those with hydroxyalkyl groups, such as hydroxypropyl cyclodextrins and/or hydroxyethyl cyclodextrins, wherein R is a " CH2- CH(OH)-CH3 or a "CH2CH2-OH group; those with (hydroxyalkyl)alkylenyl bridging groups such as cyclodextrin glycerol ethers wherein (2-hydroxyethyl)ethylenyl, - CH2CH(CH2OH)-, groups bridge between the 2' and 3' hydroxyl oxygens on the glucosyl units; branched cyclodextrins such as maltose-bonded cyclodextrins
- Cyclodextrins particularly preferred for use herein are alpha-cyclodextrin, beta- cyclodextrin, hydroxypropyl alpha-cyclodextrin, hydroxypropyl beta-cyclodextrin, methylated alpha-cyclodextrin, methylated beta-cyclodextrin, and mixtures thereof. More preferred for use herein are alpha-cyclodextrin, beta-cyclodextrin, hydroxypropyl beta-cyclodextrin, hydroxypropyl alpha-cyclodextrin, methylated beta-cyclodextrin, methylated alpha-cyclodextrin and mixtures thereof.
- Typical levels of cyclodextrin are from about 0.1 % to about 10%, preferably from about 0.2% to about 4%, more preferably from about 0.3% to about 3%, most preferably from about 0.4%> to about 2%, by weight of the composition.
- odor control agents include, but are not limited to, water soluble metallic salt, zeolites, soluble carbonate and/or bicarbonate salts, water soluble ionic polymers, silica gel, silica molecular sieves, activated alumina, kieselguhr, fullers earth, montmorillonite, smectite, attapulgite, bentonite, palygorskite, kaolinite, illite, halloysite, hectorite, beidellite, nontronite, saponite, hormite, vermiculite, sepiolite, chlorophyll, soda lime, calcium oxide, chitin, potassium permanganate, and activated charcoal or activated carbon. Mixtures of any of the above odor control agents can also be used.
- Metallic Salt water soluble metallic salt
- zeolites zeolites, soluble carbonate and/or bicarbonate salts
- water ionic polymers water soluble ionic poly
- metallic salt preferably water-soluble zinc salts
- a water-soluble metallic salt can be used as an odor control agent.
- a water-soluble metallic salt can be present in the freshening composition of the present invention to absorb amine and sulfur-containing compounds. Furthermore, they usually do not contribute an odor of their own.
- the water-soluble metallic salts are selected from the group consisting of copper salts, zinc salts, and mixtures thereof.
- the preferred zinc salts have been used most often for their ability to ameliorate malodor, e.g., in mouth wash products, as disclosed in U.S. Pat. Nos. 4,325,939, issued Apr. 20, 1982 and 4,469,674, issued Sept. 4, 1983, to N. B. Shah, et al., incorporated herein by reference.
- U.S. Pat. No. 3,172,817, issued to Leupold, et al. discloses deodorizing compositions containing slightly water-soluble salts of an acyl-acetone with a polyvalent metal, including copper and zinc salts. Said patents are incorporated herein by reference.
- Examples of preferred water-soluble zinc salts are zinc chloride, zinc gluconate, zinc lactate, zinc maleate, zinc salicylate, zinc sulfate, etc. Highly-ionized and soluble zinc salts such as zinc chloride, provide the best source of zinc ions.
- Examples of preferred copper salts are copper chloride and copper gluconate.
- Prefe ⁇ ed metallic salts are zinc chloride and copper chloride.
- Metallic salts are added to the composition of the present invention typically at a level of from about 0.1% to about 10%, preferably from about 0.2% to about 7%, more preferably from about 0.3% to about 5%, by weight of the composition.
- the pH of the solution is adjusted to less than about 7, more preferably less than about 6, most preferably, less than about 5, in order to keep the solution clear.
- Mixtures of the metallic salts and odor control agents can also be used.
- thickeners can be added to the composition of the present invention.
- suitable thickeners include, but are not limited to, naturally-occurring polymeric materials such as sodium alginate, xanthan gum, quince seed extract, tragacanth gum, starch and the like, semi-synthetic polymeric materials such as cellulose ethers (e.g.
- Inorganic thickeners may also be used such as aluminium silicates, such as, for example, bentonites, or a mixture of polyethylene glycol and polyethylene glycol stearate or distearate. Crystalline hydroxy containing waxes such as trihydroxystearin are also useful.
- hydrophilic gelling agents such as the acrylic acid/ethyl acrylate copolymers and the carboxyvinyl polymers sold by the B.F. Goodrich Company under the trademark of Carbopol Registered TM resins.
- These resins consist essentially of a colloidally water-soluble polyalkenyl polyether crosslinked polymer of acrylic acid crosslinked with from 0.75% to 2.00%) of a crosslinking agent such as polyallyl sucrose or polyally pentaerythritol.
- a crosslinking agent such as polyallyl sucrose or polyally pentaerythritol. Examples include Carbopol 934,Carbopol 940, Carbopol 950, Carbopol 980, Carbopol 951 and Carbopol 981.
- Carbopol 934 is a water-soluble polymer of acrylic acid crosslinked with about 1% of a polyallyl ether of sucrose having an average of about 5.8 allyl groups for each sucrose molecule. Also suitable for use herein are carbomers sold under the Trade Name "Carbopol Ultrez 10, Carbopol ETD2020, Carbopol 1382, Carbopol 1342, Salcare SC96 (Polyquaternium-37 and Propyl ene Glycol Dicaprylate/Dicaprate and PPG-1 Trideceth-6), Stabileze QM (Polyvinylmethacrylate/Methacrylic acid Decadiene crosspolymer), Stabylen 30 (acrylate/vinyl isodecanoate crosspolymer) and Pemulen TR-1 (CTFA Designation: Acrylates/ 10-30 Alkyl Acrylate Crosspolymer).
- gelling agents suitable for use herein include oleogels such as trihydroxystearin and aluminum magnesium hydroxy stearate.
- Another useful thickener for the present invention is the non-ionic polymer under the CTFA designation: polyacrylamide and isoparrafin and laureth-7, available as Sepigel from Seppic Corporation.
- Hydrophobically modified celluloses are also suitable for use herein. These celluloses are described in detail in U.S. Patents 4,228,277 and 5,104,646, both of which are herein incorporated by reference in their entirety.
- carbomers such as Carbopol 980, Carbopol 940, Carbopol Ultrez 10, Carbopol ETD2020 and mixtures thereof.
- the thickener is preferably present at a concentration of from about 0.01% to about 10%), preferably from about 0.1% to about 5%, more preferably from about 0.1 % to about 1% and even more preferably from about 0.1 % to about 0.5%. Mixtures of the above thickeners may also be used. Humectants
- humectants serve to retain water on the skin surface.
- preferred humectants include polyhydric alcohols selected from the group consisting of ethylene glycol, propylene glycol, dipropylene glycol, butylene glycol, hexylene glycol, polyethylene glycols, glycerin sorbitol, panthenols, urea, alkoxylated glucose derivatives, such as Glucam (RTM) E-20, hexanetriol, glucose ethers, sodium hyaluronate, soluble chitosan and mixtures thereof.
- Glycerin is presently preferred.
- the glycerin used in this invention is preferably "glycerin, USP, 99.5%o", most preferably that which is sold by Dow Chemical, Inc., Emery Industries, Inc. (under the name “Superol 99.5%”), and Procter & Gamble.
- Another preferred humectant is "DL- panthenol”, which is sold by Hoffman-Laroche.
- Yet another preferred humectant is PEG/PPG 17/6 copolymer (17 moles ethylene oxide/6 moles propylene oxide), preferably that sold by PPG/Mazer Chemicals or Union Carbide, under the names "Macol 450" and "Ucon 75-H-450".
- Still another prefe ⁇ ed humectant is phytantriol, preferably that sold by Roche.
- polyglycerylmethacrylate lubricants having a viscosity at 25o C. of 300,000 to 1,100,000 mPa.s; a specific gravity at 25o C. of 1 to 1.2 g/ml, a pH of 5.0 to 5.5; a bound water content of 33 to 58%; and, a free water content from 5 to 20%.
- Suitable polyglycerylmethacrylate lubricants are marketed by Guardian Chemical Corporation under the trademark "Lubrajel".
- the "Lubrajels” identified as “Lubrajel DV”, “Lubrajel MS”, and “Lubrajel CG” are prefe ⁇ ed in the present invention.
- Preferred Polyethylene glycols have weight average molecular weights less than about 6000.
- Humectants are preferably present in the compositions of the present invention at concentrations of from about 0.01% to about 15%, preferably from about 0.5% to about 10%), more preferably from about l%o to about 6%o.
- Antibacterial Agents are preferably present in the compositions of the present invention at concentrations of from about 0.01% to about 15%, preferably from about 0.5% to about 10%), more preferably from about l%o to about 6%o.
- compositions of the present invention can also, optionally, contain antimicrobial agents.
- Antimicrobial agents suitable for use in the compositions of the present invention are described in U.S. Patents; 5,686,089; 5,681,802, 5,607,980, 4,714,563; 4,163,800; 3,835,057; and 3,152,181; all of which are herein incorporated by reference in their entirety.
- the antimicrobial agent is preferably present at a concentration of from about 0.001 % to about 5%, more preferably 0.05% to about 1%, even more preferably from about 0.05% to about 0.5%o, and most preferably 0.1% to about 0.5%.
- Natural antibacterial actives are also useful as antimicrobial agents. These actives derive their names from their natural occurrence in plants.
- Typical natural essential oil antibacterial actives include oils of anise, lemon, orange, rosemary, wintergreen, thyme, lavender, cloves, hops, tea tree, citronella, wheat, barley, lemongrass, cedar leaf, cedarwood, cinnamon, fleagrass, geranium, sandalwood, violet, cranberry, eucalyptus, vervain, peppermint, gum benzoin, basil, fennel, fir, balsam, menthol, ocmea origanum, Hydastis carradensis, Berberidaceae daceae, Ratanhiae and Curcuma longa.
- Also included in this class of natural essential oils are the key chemical components of the plant oils which have been found to provide the antimicrobial benefit. These chemicals include, but are not limited to anethol, catechole, camphene, carvacol, eugenol, eucalyptol, ferulic acid, farnesol, hinokitiol, tropolone, limonene, menthol, methyl salicylate, thymol, terpineol, verbenone, berberine, ratanhiae extract, caryophellene oxide, citronellic acid, curcumin, nerolidol and geraniol.
- anethol catechole, camphene, carvacol, eugenol, eucalyptol, ferulic acid, farnesol, hinokitiol, tropolone, limonene, menthol, methyl salicylate, thymol, terpineol, verb
- Additional antimicrobial agents are antibacterial metal salts.
- This class generally includes salts of metals in groups 3b-7b, 8 and 3a-5a. Specifically are the salts of aluminum, zirconium, zinc, silver, gold, copper, lanthanum, tin, mercury, bismuth, selenium, strontium, scandium, yttrium, cerium, praseodymiun, neodymium, promethum, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, lutetium and mixtures thereof.
- Prefe ⁇ ed antimicrobial agents include piroctoneolamine (hereinafter Octopirox®) available from Hoechst AG; 2,4, 4'— trichloro-2 '-hydroxy diphenylether (hereinafter "TCS” or Triclosan®”) available from Ciba-Geigy Corp.; 3,4,4'-trichlorocarbanilide (hereinafter "TCC” or “Triclocarban®”) available from Bayer AG; para -chloro-meta- xylenol (hereinafter PCMX) available from Rhone Poulenc; zinc pyrithione (hereinafter "ZPT”) available from the Olin Corp.; l-phenoxypropan-2-ol available from Nippa Laboratories Ltd.; benzalkonium chlorides and/or substituted benzalkonium chlorides such as those available from Lonza under the tradename Barquat®; benzoyl peroxide, erythromycin, tetracycline, clin
- antifungal agents include, in particular compounds belonging to the imidazole class such as clotrimazole, econazole, ketoconazole or miconazole or salts thereof, polyene compounds such as amphotericin B, compounds of the allylamine family such as terbinafme, or octopirox. Also useful herein are naftifine, tolnaftate, amphotericin B, nystatin, 5-fluorocytosine, griseofulvin, and haloprogin. Mixtures of the above antifungals can also be used. A detailed discussion of antifungals as well as additional examples can be found in Remington's pharmaceutical Sciences, 17 th ed. (Alfonso R. Gennaro ed., 1985) pp. 1225-1231, herein incorporated by reference.
- the antifungal agent is preferably present at a concentration of from about 0.001% to about 5%, more preferably 0.05% to about 1%, even more preferably from about 0.05% to about 0.5%, and most preferably 0.1% to about 0.5%.
- the skin sanitizing compositions of the present invention may also contain sensates.
- sensates can be present at a level of from about 0.01%) to about 10%),typically from about 0.1%> to about 5%, and preferably from about 0.2%) to about 1%.
- the level is selected to provide the desired level of consumer perceived sensation and can be modified as desired.
- Suitable sensate technologies include menthol, eucalyptus, 3 -1-menthoxy propane- 1,2-diol, N-substituted-p-menthane- 3-carboxamides and acyclic carboxamides.
- N-substituted-p-menthane-3-carboxamides are fully described in U.S. Patent 4,136,163 to Watson et al., issued January 23, 1979 incorporated herein by reference in its entirety.
- the most prefe ⁇ ed volatile aromatic of this class is N-ethyl-p-menthane-3- carboxamide which is commercially available as WS-3 from Wilkinson Sword Limited.
- compositions of the present invention can also contain perfumes. Suitable perfumes are described in U.S. Patent 5,723,420, herein incorporated by reference in its entirety.
- Nonlimiting examples of such perfumes include benzaldehyde, benzyl acetate, cis-3-hexenyl acetate, coumarin, dihydromyrcenol, dimethyl benzyl carbinyl acetate, ethyl vanillin, eucalyptol, eugenol, iso eugenol, flor acetate, geraniol, hydroxycitronellal, koavone, linalool, methyl anthranilate, methyl beta naphthyl ketone, methyl dihydro jasmonate, nerol, nonalactone, phenyl ethyl acetate, phenyl ethyl alcohol, alpha terpineol, beta terpineol, vanillin, and mixtures thereof.
- perfumes are preferably present at concentrations of from about 0.001 %> to about 1%, more preferably
- surfactants or surface active agents are also optional, but prefe ⁇ ed.
- Surfactants can be present in amounts of from about 0.1% to about 5% by weight of the composition. It has been found that any nonionic, anionic, cationic, zwitterionic or amphoteric surfactant, can be used alone, or in combination. Numerous surface active agents or surfactants, suitable for use in the present composition, are described in detail in McCutcheon's "Emulsifiers and Detergents", 1991. Preferably, the surface active agent is present in an amount from about 1.0 to about 30.0%> by weight, based on the weight of the composition. Examples of suitable surfactants can be found in U.S. Patents 5,624,666 and 5,785,979, both of which are herein incorporated by reference in their entirety.
- emulsifying surfactants selected from the group consisting of: emulsifying surfactants having an HLB value below 12 or about 12, preferably, from about 3 to below 12 or about 12, most preferably, from about 3 to about 11 such as steareth-2, PEG-5 soya sterol oil, PEG- 10 soya sterol oil, diethanolamine cetyl phosphate, sorbitan monostearate (Span 60), diethyleneglycol monostearate, glyceryl monostearate, and mixtures thereof; emulsifying surfactants having an HLB value of 12 or above (or about 12 and above) such as Steareth-21, polyoxyethylene sorbitan tristearate (Tween 65), polyethylene glycol 20 sorbitan monostearate, polyethylene glycol 60 sorbitan monostearate, polyethylene glycol 80 sorbitan monostearate, Steareth-20, Ceteth-20, PEG-100 stea
- compositions of the present invention comprise at least one emulsifying surfactant having an HLB value below 12 (or below about 12) and at least one emulsifying surfactant having an HLB value of 12 or above (or about 12 or above).
- HLB is well known to one of ordinary skill in the art and means hydrophobic lipophilic balance. See, “The HLB System, A Time-Saving Guide to Emulsifier Selection, " ICI Americas Inc., August (1984) and McCutcheon's, Detergents and Emulsifiers, North American Edition (1987), published by Mc Publishing Co.; which list various emulsifiers useful herein. Both of these references are incorporated herein by reference in their entirety.
- the emulsifying surfactant comprises from about 0% to about 20%>, preferably from about 0.1%) to 10%., more preferably, from about 0.25%> to about 5%, most preferably, from about 0.25% to about 2.5%.
- Skin care actives may also be incorporated into the present invention.
- Such actives include: a.) Sunscreen, sunblocks and tanning compositions: Examples of suitable sunscreens, sun blocks and artificial tanning compounds can be found in U.S.
- Irritation reducing agents examples include, but ar not limited to, corticosteroids such as hydrocortisone, methylprednisolone, dexamethasone, triamcinolone acetconide, and desoxametasone; anesthetics such as benzocaine, dyclonine, lidocaine and tetracaine; antipruitics such as camphor, menthol, oatmeal (colloidal), pramoxine, benzyl alcohol, phenol, panthenol, soluble chitosan and resorcinol.
- corticosteroids such as hydrocortisone, methylprednisolone, dexamethasone, triamcinolone acetconide, and desoxametasone
- anesthetics such as benzocaine, dyclonine, lidocaine and tetracaine
- antipruitics such as camphor, menthol, oatmeal (colloidal),
- Suitable insect repellants include, but are not limited to, substituted and unsubstituted hexanediols, substituted toluamides, and synthetic or natural pyretherins.
- insect repellants include, but are not limited to, diethyltoluamide; dimethyl phthalate (DIMP); ethohexadiol (Rutgers 612); dimethyl carbate; indalone; 2,4,4'-trichloro-2'-hydroxydiphenyl ether (Irgasan DP300); salicylic acid; willow extract; N,N'-diethyl-m- toluamide("DEET"); 2-Ethyl-l,3 Hexanediol and mixtures thereof; e.) Antiinflammatory Agents; f.) Retinoids; g.) Antiandrogens; h.) Anti-oxidants/Radical Scavengers; i.) Chelators; j.) Organic hydroxy acids k.) Desquamation agents/exfoliants
- Vitamins may also be incorporated into the compositions of the invention include, but not limited to, vitamin A, pro vitamin A, vitamin B 1 , vitamin B2, vitamin B3 compounds such as niacinamide and tocopherol nicotinate, vitamin B4, vitamin B5, vitamin B6, vitamin B12, vitamin C, vitamin D, vitamin D2, vitamin D3, vitamin E, vitamin F (cis, cis-linoleic acid), vitamin KI and combinations and derivatives thereof.
- Prefe ⁇ ed vitamins include vitamins C B and E, as well as derivatives and combinations thereof.
- the invention comprises both vitamin C and vitamin E.
- the vitamins may be present in a concentration from about 0.5-50 percent by weight, preferably 0.5-10 percent by weight, based upon the total weight of the composition.
- Film Formers may be present in a concentration from about 0.5-50 percent by weight, preferably 0.5-10 percent by weight, based upon the total weight of the composition.
- film formers include, without limitation: acrylamide/sodium acrylate copolymer; ammonium acrylates copolymer; Balsam Peru; cellulose gum; ethylene/maleic anhydride copolymer; hydroxyethylcellulose; hydroxypropylcellulose; polyacrylamide; polyethylene; polyvinyl alcohol; pvm/MA copolymer (polyvinyl methylether/maleic anhydride); PVP (polyvinylpyrrolidone); maleic anhydride copolymer such as PA- 18 available from Gulf Science and Technology; PVP/hexadecene copolymer such as Ganex V-216 available from GAP Corporation; acryliclacrylate copolymer; and the like.
- film formers can be present at concentrations of from about 0.1% to about 10%) by weight of the composition with from about l%o to about 8% being prefe ⁇ ed and from about 0.1% to about 5% being most prefe ⁇ ed.
- Other Optional Ingredients The compositions of the present invention can comprise a wide range of optional ingredients.
- abrasives examples include: abrasives, anti-acne agents, anticaking agents, antioxidants, binders, biological additives, bulking agents, chelating agents, chemical additives; colorants such as those described in U.S. Patent 5,843,407 to El-Nokaly, herein incorporated by reference in its entirety; cosmetic astringents, cosmetic biocides, denaturants, drug astringents, emulsifiers, external analgesics, film formers, fragrance components, humectants, opacifying agents, plasticizers, preservatives, propellants, reducing agents, skin bleaching agents, skin-conditioning agents (emollient, humectants, miscellaneous, and occlusive), skin protectants, solvents, foam boosters, hydrotropes, solubilizing agents, suspending agents (nonsurfactant), sunscreen agents, ultraviolet light absorbers, and viscosity increasing agents (aqueous and nonaqueous).
- compositions of the present invention can also be, optionally, incorporated into a insoluble substrate for application to the skin such as in the form of a treated wipe.
- a insoluble substrate for application to the skin
- Suitable water insoluble substrate materials and methods of manufacture are described in Riedel, "Nonwoven Bonding Methods and Materials," Nonwoven World (1987); The Encyclopedia Americana, vol. 11, pp. 147-153, vol. 21, pp. 376-383, and vol. 26, pp. 566-581 (1984); U.S. Patent No. 4,891,227, to Thaman et al, issued January 2, 1990; U.S. Patent No. 4,891,228 and U.S. Patents 5,686,088 to Mitra et al., issued November 11,1997; U.S.
- Patent 2,862,251 and Griswold U.S. Patent 3,025,585, all of which describe hydroentangling procedures generally and all of which are herein incorporated by reference. See also U.S. Patent 5,674,591 ; James et al; issued October 7, 1997 which specifically describes a hydroentangling process, including the apparatus used in said process, which can be used to prepare the patterned web.
- U.S. Patent 5,674,591 is incorporated herein in its entirety. Methods for Disinfecting and Moisturizing the Skin
- the skin sanitizing compositions of the present invention are useful for moisturizing and sanitizing the skin.
- the skin disinfection and moisturing process involves topically applying to the skin a safe and effective amount of a composition of the present invention.
- the present invention can be used when cleansing processes requiring soap and water are unavailable or inconvenient or, alternatively, applied and rinsed off with water.
- the amount of the composition applied, the frequency of application and the period of use will vary widely depending upon the level of disinfection and moisturization desired, e.g., the degree of microbial contamination and/or degree of skin dryness.
- Typical amounts of skin sanitizing composition used preferably range from about 0.1 mg/cm ⁇ to about 20 mg/cm ⁇ , more preferably from about 0.5 mg/c ⁇ r-2 to about 10 mg/cin ⁇ , and most preferably about 1 mg/ cm ⁇ to about 5 mg/cm ⁇ of skin area to be cleansed.
- the skin sanitizing compositions of the present invention are used to sanitize and moisturize human and/or animal hands and/or feet.
- compositions of the present invention can be applied by use of a patch.
- a patch can be occlusive, semi-occlusive or non-occlusive.
- the compositions and actives of the present invention can be contained within the patch or be applied to the skin prior to application of the patch.
- the patch can also include additional actives such as chemical initiators for exothermic reactions such as those described in PCT application WO 9701313 to Burkett et al.
- the patch is applied at night as a form of night therapy. Examples of useful transdermal systems are described in U.S.
- the present invention also relates to an article of manufacture comprising a dispensing container containing the moisturizing and sanitizing composition.
- Said dispensing container can be constructed of any of the conventional material employed in fabricating containers, including, but not limited to: polyethylene; polypropylene; polyacetal; polycarbonate; polyethyleneterephthalate; polyvinyl chloride; polystyrene; blends of polyethylene, vinyl acetate, and rubber elastomer. Other materials can include stainless steel and glass.
- a prefe ⁇ ed container is made of clear material, e.g., polyethylene terephthalate.
- the dispensing container of the present invention preferably contains instructions for moisturizing and conditioning the skin during the skin sanitation process, wherein the instructions instruct the user to apply the compositions of the present invention to the skin (e.g., the hands) at least 3 times a day, more preferably 5 times a day, most preferably at least 10 times a day.
- a spray dispenser is any of the manually activated means for producing a spray of liquid droplets as is known in the art.
- Particularly prefe ⁇ ed for use herein are spray dispensers equipped with an electrostatic spray device. Examples of such spray devices are found in U.S.
- a prefe ⁇ ed spray container is made of clear material, e.g., polyethylene terephthalate.
- compositions can be prepared by conventional formulation and mixing techniques.
- Component amounts are listed as weight percents and exclude minor materials such as diluents, filler, and so forth.
- the listed formulations therefore, comprise the listed components and any minor materials associated with such components.
- Example I The following is an example of a sanitizing and moisturizing gel of the present invention.
- a lipid premix is prepared by adding Stabylen 30 to water (about 15% of the total formula weight) with stirring and mixing until homogeneous. Next, petrolatum is added and the mixture is heated to 120°F and mixed to form a homogeneous melt. The melt is cooled to about 100°F and then the SFE839 elastomer dispersion is added with mixing until the premix is homogeneous.
- Carbopol Ultrez 10 is slowly added with stirring to water (about 12.98%) of the total formula weight) at about 25°C and mixed mixed until the consistency is smooth and homogeneous.
- the ethanol, ispropanol, perfume and Tospearl 145 A are added with mixing.
- the Quadrol Polyol is, then, added to form a thickened gel.
- the contents of the two vessels are slowly added together and mixed until homogeneous to form moisturizing sanitizing compositions which reduce the greasiness of the lipophilic moisturizer (i.e., petrolatum).
- the lipophilic moisturizer i.e., petrolatum
- a lipid premix is prepared by adding Stabylen 30 to water (about 15%o of the total formula weight ) with stirring and mixing until homogeneous. Next, petrolatum is added and the mixture is heated to 120°F and mixed to form a homogeneous melt. The melt is cooled to about 100°F at which time the TiO 2 and SFE839 elastomer dispersion are added and mixed in until the premix is homogeneous.
- Carbopol Ultrez 10 is slowly added with stirring to water (about 12.88%) of the total formula weight) at about 25°C and mixed until the consistency is smooth and homogeneous.
- the ethanol, ispropanol, perfume, and Tospearl 145 A are added with mixing.
- the Quadrol Polyol is, then, added to form a thickened gel.
- the contents of the two vessels are slowly added together and mixed until homogeneous to form moisturizing sanitizing compositions which reduce the greasiness of the lipophilic moisturizer (i.e., petrolatum).
- the lipophilic moisturizer i.e., petrolatum
- Example III The following is an example of a sanitizing and moisturizing gel of the present invention.
- a lipid premix is prepared by adding Stabylen 30 to water (about 15%) of the total formula weight ) with stirring and mixing until homogeneous. Next, petrolatum is added and the mixture is heated to 120°F and mixed to form a homogeneous melt. The melt is cooled to about 100°F at which time the SF1202 (D5) silicone fluid is added and mixed in until the premix is homogeneous.
- Carbopol Ultrez 10 is slowly added with stirring to water (about 13.58% of the total formula weight) at about 25°C and mixed until the consistency is smooth and homogeneous.
- the Biowax 754, ethanol, ispropanol, and perfume are added with mixing.
- the Quadrol Polyol is, then, added to form a thickened gel.
- Example -V The following is an example of a sanitizing and moisturizing gel of the present invention.
- a lipid premix is prepared by adding
- Stabylen 30 to water (about 15% of the total formula weight ) with stirring and mixing until homogeneous.
- petrolatum is added and the mixture is heated to 120°F and mixed to form a homogeneous melt.
- the melt is cooled to about 100°F at which time the
- Carbopol Ultrez 10 is slowly added with stirring to water (about 9.58% of the total formula weight) at about 25°C and mixed until the consistency is smooth and homogeneous.
- the Biowax 754, glycerin, ethanol, ispropanol, Tospearl 145 A and perfume are added with mixing.
- the Quadrol Polyol is, then, added to form a thickened gel.
- the contents of the two vessels are slowly added together and mixed until homogeneous to form moisturizing sanitizing compositions which reduce the greasiness of the lipophilic moisturizer (i.e., petrolatum).
- the lipophilic moisturizer i.e., petrolatum
- Example V The following is an example of a sanitizing and moisturizing gel of the present invention.
- a lipid premix is prepared by adding Stabylen 30 to water (about 15% of the total formula weight ) with stirring and mixing until homogeneous. Next, petrolatum is added and the mixture is heated to 120°F and mixed to form a homogeneous melt. The melt is cooled to about 100°F at which time the SFE839 Elastomer dispersion is added and mixed in until the premix is homogeneous.
- Carbopol Ultrez 10 is slowly added with sti ⁇ ing to water (about 15.08% of the total formula weight) at about 25°C and mixed until the consistency is smooth and homogeneous.
- the Biowax 754, ethanol, ispropanol, Tospearl 145 A and perfume are added with mixing.
- the Quadrol Polyol is, then, added to form a thickened gel.
- the contents of the two vessels are slowly added together and mixed until homogeneous to form moisturizing sanitizing compositions which reduce the greasiness of the lipophilic moisturizer (i.e., petrolatum).
- the lipophilic moisturizer i.e., petrolatum
- Example VI The following is an example of a sanitizing and moisturizing gel of the present invention.
- a lipid premix is prepared by adding Stabylen 30 to water (about 15% of the total formula weight ) with stirring and mixing until homogeneous. Next, petrolatum is added and the mixture is heated to 120°F and mixed to form a homogeneous melt. The melt is cooled to about 100°F at which time the SFE839 Elastomer dispersion is added and mixed in until the premix is homogeneous.
- Carbopol Ultrez 10 is slowly added with stirring to water (about 4.58%o of the total formula weight) at about 25°C and mixed until the consistency is smooth and homogeneous.
- the Biowax 754, glycerin, ethanol, ispropanol, Tospearl 145 A and perfume are added with mixing.
- the Quadrol Polyol is, then, added to form a thickened gel.
- the contents of the two vessels are slowly added together and mixed until homogeneous to form moisturizing sanitizing compositions which reduce the greasiness of the lipophilic moisturizer (i.e., petrolatum).
- the lipophilic moisturizer i.e., petrolatum
- a lipid premix is prepared by adding Stabylen 30 to water (about 15 > of the total formula weight) with stirring and mixing until homogeneous. Next, petrolatum is added and the mixture is heated to 120°F and mixed to form a homogeneous melt. The melt is cooled to about 100°F and then the SFE839 elastomer dispersion is added with mixing until the premix is homogeneous.
- Carbopol Ultrez 10 is slowly added with stirring to water (about 8.98%o of the total formula weight) at about 25°C and mixed mixed until the consistency is smooth and homogeneous.
- water about 8.98%o of the total formula weight
- the ethanol, ispropanol, perfume and Tospearl 145 A are added with mixing.
- the Quadrol Polyol is, then, added to form a thickened gel.
- the contents of the two vessels are slowly added together and mixed until homogeneous to form moisturizing sanitizing compositions which reduce the greasiness of the lipophilic moisturizer (i.e., petrolatum).
- the lipophilic moisturizer i.e., petrolatum
Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP00908591A EP1152743B1 (en) | 1999-02-12 | 2000-02-10 | Skin sanitizing compositions |
MXPA01008159A MXPA01008159A (en) | 1999-02-12 | 2000-02-10 | Skin sanitizing compositions. |
AU29904/00A AU2990400A (en) | 1999-02-12 | 2000-02-10 | Skin sanitizing compositions |
DE60014035T DE60014035D1 (en) | 1999-02-12 | 2000-02-10 | COMPOSITION FOR SKIN DISINFECTION |
AT00908591T ATE276735T1 (en) | 1999-02-12 | 2000-02-10 | COMPOSITION FOR SKIN DISINFECTION |
JP2000598137A JP2002536398A (en) | 1999-02-12 | 2000-02-10 | Skin antiseptic composition |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US24920999A | 1999-02-12 | 1999-02-12 | |
US09/249,209 | 1999-02-12 | ||
US09/320,997 US6183766B1 (en) | 1999-02-12 | 1999-05-27 | Skin sanitizing compositions |
US09/320,997 | 1999-05-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000047184A1 true WO2000047184A1 (en) | 2000-08-17 |
Family
ID=26939905
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2000/003511 WO2000047184A1 (en) | 1999-02-12 | 2000-02-10 | Skin sanitizing compositions |
Country Status (9)
Country | Link |
---|---|
US (1) | US6183766B1 (en) |
EP (1) | EP1152743B1 (en) |
JP (1) | JP2002536398A (en) |
CN (1) | CN1343115A (en) |
AT (1) | ATE276735T1 (en) |
AU (1) | AU2990400A (en) |
DE (1) | DE60014035D1 (en) |
MX (1) | MXPA01008159A (en) |
WO (1) | WO2000047184A1 (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1151744A1 (en) * | 2000-05-05 | 2001-11-07 | Laboratoire Nuxe | Cosmetic and/or dermatologic composition with enhanced stability |
GB2369052A (en) * | 2000-09-12 | 2002-05-22 | Barrier Biotech Ltd | Antimicrobial compositions comprising a blend of essential oils |
WO2002047639A2 (en) * | 2000-12-12 | 2002-06-20 | The Procter & Gamble Company | Single-phase antiperspirant compositions containing silicone elastomer |
WO2002051379A2 (en) * | 2000-12-23 | 2002-07-04 | Impetus Ag | Thixotropic nasal spray |
DE10226349A1 (en) * | 2002-06-13 | 2003-12-24 | Beiersdorf Ag | Cosmetic and dermatological light protection preparations containing a combination of UV absorbers and spherical silicon oxides |
CN102885697A (en) * | 2011-07-22 | 2013-01-23 | 陈进民 | Inflammation diminishing and sterilizing flower perfume and preparation method thereof |
DE10296678B4 (en) * | 2001-04-18 | 2014-03-27 | Kimberly-Clark Worldwide, Inc. | Anionic carboxymethylcellulose particle-containing skin cleansing composition |
US9717669B2 (en) | 2012-07-23 | 2017-08-01 | Innovative Biodefense, Inc. | Topical sanitizing formulations and uses thereof |
WO2020126347A1 (en) * | 2018-12-18 | 2020-06-25 | Unilever N.V. | An antimicrobial composition |
DE102018133179A1 (en) * | 2018-12-20 | 2020-06-25 | Brauns-Heitmann Gmbh & Co Kg | Disinfectant composition |
WO2021219622A1 (en) * | 2020-04-30 | 2021-11-04 | Dsm Ip Assets B.V. | Hand sanitiser composition |
EP3206487B1 (en) | 2014-10-16 | 2021-12-29 | Schülke & Mayr GmbH | Use of fatty acid ester for improving the antimicrobial efficacy of an alcoholic disinfectant |
RU2769876C1 (en) * | 2018-10-31 | 2022-04-07 | ЮНИЛЕВЕР АйПи ХОЛДИНГС Б. В. | Antimicrobial composition |
Families Citing this family (155)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6623744B2 (en) * | 1995-06-22 | 2003-09-23 | 3M Innovative Properties Company | Stable hydroalcoholic compositions |
CA2224798A1 (en) * | 1995-06-22 | 1997-01-09 | Matthew T. Scholz | Stable hydroalcoholic compositions |
US7566460B2 (en) * | 1995-06-22 | 2009-07-28 | 3M Innovative Properties Company | Stable hydroalcoholic compositions |
US6582711B1 (en) * | 1997-01-09 | 2003-06-24 | 3M Innovative Properties Company | Hydroalcoholic compositions thickened using polymers |
JP4090197B2 (en) | 1997-09-26 | 2008-05-28 | 株式会社クレハ | Microbial pesticides |
US6358516B1 (en) * | 1998-08-21 | 2002-03-19 | Norris R. Harod | One-step system for cleansing, conditioning, and treating the skin |
US6423329B1 (en) * | 1999-02-12 | 2002-07-23 | The Procter & Gamble Company | Skin sanitizing compositions |
US6515029B1 (en) | 1999-04-23 | 2003-02-04 | Kimberly-Clark Worldwide, Inc. | Absorbent article having a hydrophilic lotionized bodyside liner |
US6200964B1 (en) * | 1999-05-28 | 2001-03-13 | Neutrogena Corporation | Silicone gel containing salicylic acid |
US6719961B1 (en) * | 1999-12-07 | 2004-04-13 | Cognis Corporation | Use of chitosan to decrease skin irritation caused by shaving |
US6503517B1 (en) * | 2000-01-28 | 2003-01-07 | Conopco, Inc. | Cosmetic compositions with menthol |
US6706364B2 (en) | 2000-03-14 | 2004-03-16 | Ossur Hf | Composite elastic material |
EP1263356B1 (en) * | 2000-03-14 | 2010-01-27 | Ossur HF | Apparatus and process for making prosthetic suction sleeve |
MXPA02011440A (en) * | 2000-05-23 | 2003-04-25 | Unilever Nv | Deodorant and or antiperspirant compositions. |
US6468989B1 (en) * | 2000-07-13 | 2002-10-22 | Dow Pharmaceutical Sciences | Gel compositions containing metronidazole |
US6409997B1 (en) * | 2000-07-31 | 2002-06-25 | Neutrogena Corporation | Wax cosmetic stick |
US6702951B2 (en) | 2000-10-06 | 2004-03-09 | Robinson Laboratories, Inc. | Scent adsorbing liquid formulation |
US6756520B1 (en) | 2000-10-20 | 2004-06-29 | Kimberly-Clark Worldwide, Inc. | Hydrophilic compositions for use on absorbent articles to enhance skin barrier |
US6503526B1 (en) | 2000-10-20 | 2003-01-07 | Kimberly-Clark Worldwide, Inc. | Absorbent articles enhancing skin barrier function |
US6617294B2 (en) * | 2000-10-20 | 2003-09-09 | Vinod K. Narula | Waterless sanitizing hand cleanser |
AU2002215331A1 (en) * | 2000-10-20 | 2002-05-06 | Dipak Narula | Sanitizing hand cleanser |
JP2002179509A (en) * | 2000-12-12 | 2002-06-26 | Takasago Internatl Corp | Antifugal perfume composition |
US20020120242A1 (en) * | 2000-12-22 | 2002-08-29 | Tyrrell David John | Absorbent articles with hydrophilic compositions containing botanicals |
US20020128615A1 (en) * | 2000-12-22 | 2002-09-12 | Tyrrell David John | Absorbent articles with non-aqueous compositions containing anionic polymers |
US6749860B2 (en) | 2000-12-22 | 2004-06-15 | Kimberly-Clark Worldwide, Inc. | Absorbent articles with non-aqueous compositions containing botanicals |
US7771735B2 (en) * | 2000-12-22 | 2010-08-10 | Kimberly-Clark Worldwide, Inc. | Absorbent articles with compositions for reducing irritation response |
US20020120241A1 (en) * | 2000-12-22 | 2002-08-29 | Tyrrell David John | Absorbent articles with hydrophilic compositions containing anionic polymers |
JP2002212060A (en) * | 2001-01-18 | 2002-07-31 | Tsumura & Co | Detergent composition |
US20020102229A1 (en) * | 2001-01-29 | 2002-08-01 | Paul Wegner | Product for and method of controlling odor |
GB0105229D0 (en) | 2001-03-02 | 2001-04-18 | Ectopharma Ltd | Pesticides |
DE10121466A1 (en) * | 2001-05-02 | 2002-11-14 | Rainer Eckardt | Ointment for treating dry and inflamed nasal mucosa comprises olive oil, dexpanthenol, an oily carrier and an ointment base |
AU2002317981B2 (en) * | 2001-07-24 | 2006-12-07 | Advanced Biotechnologies | Topical pharmaceutical formulation |
US6929800B2 (en) | 2001-08-06 | 2005-08-16 | Abdul Rasoul Salman | Nasal passage cleaning composition |
US6497894B1 (en) * | 2001-08-06 | 2002-12-24 | Dow Corning Corporation | Aqueous dispersion of cured silicone rubber particles |
US6756059B2 (en) * | 2001-08-20 | 2004-06-29 | Skinvisible Pharmaceuticals, Inc. | Topical composition, topical composition precursor, and methods for manufacturing and using |
US6846846B2 (en) * | 2001-10-23 | 2005-01-25 | The Trustees Of Columbia University In The City Of New York | Gentle-acting skin disinfectants |
US20050163846A1 (en) * | 2001-11-21 | 2005-07-28 | Eisai Co., Ltd. | Preparation composition containing acid-unstable physiologically active compound, and process for producing same |
US6806213B2 (en) * | 2001-12-20 | 2004-10-19 | Kimberly-Clark Worldwide, Inc. | Disposable wash cloth and method of using |
US20030130636A1 (en) * | 2001-12-22 | 2003-07-10 | Brock Earl David | System for improving skin health of absorbent article wearers |
US20030130635A1 (en) * | 2001-12-22 | 2003-07-10 | Tate Martha Lillian | Absorbent articles with compositions having even distribution |
US6881726B2 (en) * | 2001-12-24 | 2005-04-19 | Dow Pharmaceutical Sciences | Aqueous compositions containing metronidazole |
US7879365B2 (en) * | 2002-02-07 | 2011-02-01 | The Trustees Of Columbia University In The City Of New York | Zinc salt compositions for the prevention of dermal and mucosal irritation |
AU2003216213B2 (en) * | 2002-02-07 | 2008-10-02 | The Trustees Of Columbia University In The City Of New York | Zinc salt compositions for the prevention of mucosal irritation from spermicides and microbicides |
US7745425B2 (en) * | 2002-02-07 | 2010-06-29 | The Trustees Of Columbia University In The City Of New York | Non-irritating compositions containing zinc salts |
AU2003209436A1 (en) * | 2002-02-08 | 2003-09-02 | The Procter & Gamble Company | Rinse-off skin conditioning compositions |
KR20030077087A (en) * | 2002-03-25 | 2003-10-01 | 한불화장품주식회사 | Silicon in water emulsion type cosmetic composition |
FR2838295B1 (en) * | 2002-04-15 | 2005-05-13 | Georgia Pacific France | USE OF GLUCONATE METAL SALTS FOR THE MANUFACTURE OF SUBSTRATES WITH ANTIMICROBIAL ACTIVITY |
US20030211069A1 (en) | 2002-05-09 | 2003-11-13 | The Procter & Gamble Company | Rinsable skin conditioning compositions |
WO2004022024A1 (en) * | 2002-09-07 | 2004-03-18 | Johnson & Johnson Consumer France S.A.S. | Compositions comprising soy products and organic salts of certain metals |
FR2844707B1 (en) * | 2002-09-19 | 2006-05-12 | Oreal | WIPES AND USES WITHOUT THE COSMETIC DOMAIN |
ATE546521T1 (en) * | 2002-10-04 | 2012-03-15 | Firmenich & Cie | SESQUITERPENE SYNTHASES AND METHODS OF USE |
US7488471B2 (en) * | 2002-10-28 | 2009-02-10 | Mmp, Inc. | Transparent oil-in-water emulsion |
KR20040051870A (en) * | 2002-12-13 | 2004-06-19 | 주식회사 엘지생활건강 | Body rinse composition |
US20040126339A1 (en) * | 2002-12-31 | 2004-07-01 | Roszell James A. | Sunscreen composition and methods for manufacturing and using a sunscreen composition |
DE10301836A1 (en) * | 2003-01-20 | 2004-07-29 | Beiersdorf Ag | Cosmetic or dermatological preparations with a pearlescent look |
US20040185022A1 (en) * | 2003-02-19 | 2004-09-23 | Steven Rubin | Regimen for acne treatment |
PL1622576T3 (en) * | 2003-05-07 | 2007-06-29 | Firmenich & Cie | Sprayable perfume with an improved tenacity |
AU2004238310A1 (en) * | 2003-05-08 | 2004-11-25 | The Procter & Gamble Company | Personal care compositions containing a silicone elastomer and a dispersed oil phase |
CN100408022C (en) * | 2003-05-08 | 2008-08-06 | 宝洁公司 | Personal care compositions containing a silicone elastomer and a dispersed oil phase |
US20040234478A1 (en) * | 2003-05-08 | 2004-11-25 | The Procter & Gamble Company | Personal care compositions containing a silicone elastomer |
US20040223992A1 (en) * | 2003-05-09 | 2004-11-11 | The Procter & Gamble Company | Wet skin treatment compositions comprising gel-networks |
US20050025817A1 (en) * | 2003-07-03 | 2005-02-03 | Bhatia Kuljit S. | Delivery system for topical medications |
US7776355B2 (en) * | 2003-07-03 | 2010-08-17 | Medics Pharmaceutical Corporation | Delivery system for topical medications |
CN102309473A (en) * | 2003-07-17 | 2012-01-11 | 纽约市哥伦比亚大学托管会 | Antimicrobial compositons containing synergistic combinations of quaternary ammonium compounds and essential oils and/or constituents thereof |
US6875453B2 (en) * | 2003-07-18 | 2005-04-05 | Manuel Viamonte, Jr. | Non-toxic disinfectant containing a isopropyl alcohol and sesame oil composition with lemon oil and menthol |
GB0318160D0 (en) * | 2003-08-02 | 2003-09-03 | Ssl Int Plc | Parasiticidal composition |
KR20060113907A (en) * | 2003-09-29 | 2006-11-03 | 에테나 헬스케어 인코포레이티드 | - high alcohol content gel-like and foaming compositions |
GB0323754D0 (en) * | 2003-10-10 | 2003-11-12 | Reckitt Benckiser Uk Ltd | Article and method |
US9359585B2 (en) * | 2003-12-08 | 2016-06-07 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Stable nonaqueous reactive skin care and cleansing compositions having a continuous and a discontinuous phase |
US20050123487A1 (en) * | 2003-12-08 | 2005-06-09 | Spadini Alessandro L. | Stable nonaqueous liquid reactive skin care and cleansing packaged product |
US7846462B2 (en) | 2003-12-22 | 2010-12-07 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Personal care implement containing a stable reactive skin care and cleansing composition |
NZ549838A (en) * | 2004-03-26 | 2010-04-30 | Eisai R&D Man Co Ltd | Coated controlled-release preparation containing a gastric acid secretion inhibitor |
US20050244522A1 (en) * | 2004-04-30 | 2005-11-03 | Carrara Dario Norberto R | Permeation enhancer comprising genus Curcuma or germacrone for transdermal and topical administration of active agents |
US20050271710A1 (en) * | 2004-06-04 | 2005-12-08 | Argo Brian P | Antimicrobial tissue products with reduced skin irritation potential |
US7479289B2 (en) * | 2004-07-02 | 2009-01-20 | Medicis Pharmaceutical Corporation | Stable cleanser compositions containing sulfur |
US7655682B2 (en) * | 2004-07-02 | 2010-02-02 | Medicis Pharmaceutical Corporation | Triple anti-irritant composition |
US7268165B2 (en) * | 2004-08-20 | 2007-09-11 | Steris Inc. | Enhanced activity alcohol-based antimicrobial compositions |
US20060047005A1 (en) * | 2004-08-26 | 2006-03-02 | Salamone Joseph C | Compositions containing N,N,N',N'-tetrakis(hydroxyalkyl)diamine-or N,N,N',N'-tetrakis(hydroxyalkoxy)diamine-based buffers |
US20060074029A1 (en) * | 2004-10-04 | 2006-04-06 | Scott Leece | Topical antimicrobial composition having improved moisturization properties |
TWI348919B (en) * | 2004-12-07 | 2011-09-21 | Access Business Group Int Llc | Methods for scavenging oxidizing nitrogen and oxygen species with fragrances having anti-oxidative properties |
DE102004062775A1 (en) | 2004-12-21 | 2006-06-29 | Stockhausen Gmbh | Alcoholic pump foam |
AU2005323206C1 (en) * | 2005-01-04 | 2010-01-07 | Teikoku Pharma Usa, Inc. | Cooling topical patch preparation |
US8147853B2 (en) * | 2005-02-15 | 2012-04-03 | The Procter & Gamble Company | Personal care compositions containing hydrophobically modified non-platelet particles |
MX2007007305A (en) * | 2005-03-04 | 2007-07-09 | Procter & Gamble | Rinse-off or wipe-off skin cleansing compositions. |
AU2006222502B2 (en) * | 2005-03-07 | 2010-02-11 | Deb Ip Limited | High alcohol content foaming compositions with silicone-based surfactants |
US20060204466A1 (en) * | 2005-03-08 | 2006-09-14 | Ecolab Inc. | Hydroalcoholic antimicrobial composition with skin health benefits |
JP2006282629A (en) * | 2005-04-04 | 2006-10-19 | Taiko:Kk | Spray composition |
US20060275241A1 (en) * | 2005-06-06 | 2006-12-07 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Cosmetic towelette product |
US8512724B2 (en) | 2005-06-10 | 2013-08-20 | The Board Of Regents Of The University Of Texas System | Antiseptic compositions |
US7651990B2 (en) * | 2005-06-13 | 2010-01-26 | 3M Innovative Properties Company | Foamable alcohol compositions comprising alcohol and a silicone surfactant, systems and methods of use |
US20070027152A1 (en) * | 2005-07-27 | 2007-02-01 | Clark Kathleen L | Topical anti-pruritic compositions and methods of action of same |
US20070027153A1 (en) * | 2005-07-27 | 2007-02-01 | Reeth Kevin M | Topical skin-protectant and anti-pruritic compositions |
EP1930030A1 (en) * | 2005-09-29 | 2008-06-11 | Eisai R&D Management Co., Ltd. | Pulse preparation having improved disintegration properties in vivo |
MX2008000486A (en) * | 2005-10-24 | 2008-03-07 | Teikoku Pharma Usa Inc | Topical pain relief compositions of n,2,3-trimethyl-2-isopropylbu tamide and methods for using the same. |
US20070148101A1 (en) * | 2005-12-28 | 2007-06-28 | Marcia Snyder | Foamable alcoholic composition |
US7759327B2 (en) | 2006-01-06 | 2010-07-20 | The Trustees Of Columbia University In The City Of New York | Compositions containing zinc salts for coating medical articles |
US8119115B2 (en) | 2006-02-09 | 2012-02-21 | Gojo Industries, Inc. | Antiviral method |
US20070185216A1 (en) * | 2006-02-09 | 2007-08-09 | Marcia Snyder | Antiviral method |
US8450378B2 (en) * | 2006-02-09 | 2013-05-28 | Gojo Industries, Inc. | Antiviral method |
MX2008010716A (en) | 2006-02-21 | 2008-10-14 | Mary Kay Inc | Stable vitamin c compositions. |
US20100105738A1 (en) * | 2006-10-06 | 2010-04-29 | Mitsuru Mizuno | Extended release formulations of a proton pump inhibitor |
WO2008066618A2 (en) * | 2006-10-20 | 2008-06-05 | Skinvisible Pharmaceuticals, Inc. | Antifungal composition and methods for using |
US7419012B2 (en) * | 2006-10-26 | 2008-09-02 | Varco I/P, Inc. | Wellbore top drive systems |
EP1930500A1 (en) * | 2006-12-08 | 2008-06-11 | Cognis IP Management GmbH | Emulsions for the softening of textiles and paper |
JP4602999B2 (en) * | 2007-01-29 | 2010-12-22 | 花王株式会社 | Cleansing composition |
US7790202B1 (en) * | 2007-04-09 | 2010-09-07 | Martell Helen D | Multi-purpose skin composition |
US8333954B2 (en) * | 2007-04-30 | 2012-12-18 | Kimberly-Clark Worldwide, Inc. | Foamable sanitizing compositions |
US8128913B1 (en) | 2007-12-06 | 2012-03-06 | Skinvisible Pharmaceuticals, Inc. | Sunscreen composition with enhanced UV-A absorber stability and methods |
US10589134B2 (en) * | 2008-01-30 | 2020-03-17 | Kimberly-Clark Worldwide, Inc. | Hand health and hygiene system for hand health and infection control |
US8840911B2 (en) * | 2008-03-07 | 2014-09-23 | Kimberly-Clark Worldwide, Inc. | Moisturizing hand sanitizer |
US8299122B2 (en) * | 2008-04-14 | 2012-10-30 | Skinvisible Pharmaceuticals, Inc. | Method for stabilizing retinoic acid, retinoic acid containing composition, and method of using a retinoic acid containing composition |
US7842725B2 (en) | 2008-07-24 | 2010-11-30 | Ecolab USA, Inc. | Foaming alcohol compositions with selected dimethicone surfactants |
EA019846B1 (en) * | 2008-10-20 | 2014-06-30 | Юнилевер Нв | An antimicrobial composition, comprising thymol and terpineol, and use thereof |
US20100317640A1 (en) * | 2009-05-01 | 2010-12-16 | Microban Products Company | Antimicrobial zinc pyrithione composition and method |
TW201113091A (en) * | 2009-06-15 | 2011-04-16 | Gojo Ind Inc | Methods and compositions for use with gel dispensers |
US20100322875A1 (en) * | 2009-06-18 | 2010-12-23 | Advanced Bio-Technologies, Inc. | Silicone scar treatment preparation |
EP2480090B1 (en) | 2009-09-24 | 2013-11-06 | Unilever NV | Disinfecting agent comprising eugenol, terpineol and thymol |
CA2779433A1 (en) * | 2009-11-03 | 2011-05-12 | Lipidor Ab | Composition for promoting wound healing |
DE102010004950A1 (en) * | 2010-01-18 | 2011-07-21 | Remis Gesellschaft für Entwicklung und Vertrieb von technischen Elementen mbH, 50829 | Cooling shelf with door device |
US7951766B1 (en) * | 2010-02-12 | 2011-05-31 | Galata Chemicals, Llc | Bio-based solvents and methods for using same |
EP2373066B1 (en) * | 2010-03-16 | 2017-08-02 | Rasco GmbH | Microelectromechanical system testing device |
US20130061865A1 (en) * | 2010-05-31 | 2013-03-14 | Sameer Keshav Barne | Skin treatment composition |
EP2648681B1 (en) | 2010-12-07 | 2015-01-07 | Unilever N.V. | An oral care composition |
WO2013064360A2 (en) | 2011-11-03 | 2013-05-10 | Unilever N.V. | A personal cleaning composition |
JP6182975B2 (en) * | 2013-05-21 | 2017-08-23 | 日油株式会社 | Gel skin cosmetic |
US9439841B2 (en) | 2013-06-06 | 2016-09-13 | Ecolab Usa Inc. | Alcohol based sanitizer with improved dermal compatibility and feel |
MX2016002481A (en) * | 2013-09-05 | 2016-05-31 | Procter & Gamble | Hair care compositions comprising viscoelastic particle. |
JP6399645B2 (en) * | 2013-09-10 | 2018-10-03 | 花王株式会社 | Hand sanitizer composition |
US9782887B2 (en) * | 2013-11-17 | 2017-10-10 | Kimberly D. Jaskolski | Grip enhancing composition and method of use |
US9226890B1 (en) | 2013-12-10 | 2016-01-05 | Englewood Lab, Llc | Polysilicone base for scar treatment |
WO2015100122A1 (en) | 2013-12-23 | 2015-07-02 | Lubrizol Advanced Materials, Inc. | Suspension and stability agent for antidandruff hair care compositions |
JP6734781B2 (en) * | 2014-03-14 | 2020-08-05 | ゴジョ・インダストリーズ・インコーポレイテッド | Hand sanitizer with improved aesthetics and skin conditioning to encourage adherence to hand hygiene guidelines |
WO2015183833A1 (en) * | 2014-05-26 | 2015-12-03 | The Regents Of The University Of California | Organic pruning wound composition |
US20160000858A1 (en) | 2014-07-07 | 2016-01-07 | Gojo Industries, Inc. | Compositions and methods for mitigating skin irritation and enhancing skin barrier function |
US10912719B2 (en) | 2014-10-20 | 2021-02-09 | The Procter And Gamble Company | Personal care composition and method of making |
US9868887B1 (en) * | 2014-11-17 | 2018-01-16 | Kimberly D. Jaskolski | Grip enhancing composition |
KR20170095373A (en) | 2014-12-18 | 2017-08-22 | 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 | Amphiphilic suspension and stability agent for antidandruff hair care compositions |
WO2017066288A1 (en) * | 2015-10-13 | 2017-04-20 | Practical Solution, Inc. | Topical formulations for preventing skin infection |
JP2019501260A (en) | 2015-12-23 | 2019-01-17 | ルブリゾル アドバンスド マテリアルズ, インコーポレイテッド | Hydrophobic modified alkali swellable emulsion polymer |
US10945935B2 (en) | 2016-06-27 | 2021-03-16 | The Procter And Gamble Company | Shampoo composition containing a gel network |
EP3606343A1 (en) | 2017-04-04 | 2020-02-12 | Gojo Industries Inc | Methods and compounds for increasing virucidal efficacy in hydroalcoholic systems |
EA202091454A1 (en) | 2018-01-08 | 2020-10-09 | Юнилевер Н.В. | COSMETIC COMPOSITIONS CONTAINING SILICONE ELASTOMER AND SOFTENING COMPONENT |
CA3093321A1 (en) * | 2018-03-13 | 2019-09-19 | Unilever Plc | A sanitizer composition |
WO2019215679A1 (en) | 2018-05-10 | 2019-11-14 | Protair-X Health Solutions, Inc. | Foam sanitizer composition |
CN112261931B (en) | 2018-06-05 | 2023-12-08 | 宝洁公司 | Transparent cleaning composition |
KR102181100B1 (en) * | 2018-12-03 | 2020-11-20 | 주식회사 이도팜 | Alcohl swab for preventing infection |
JP7328336B2 (en) | 2018-12-14 | 2023-08-16 | ザ プロクター アンド ギャンブル カンパニー | SHAMPOO COMPOSITION CONTAINING SHEET-FORMED MICROCAPSULES |
US11896689B2 (en) | 2019-06-28 | 2024-02-13 | The Procter & Gamble Company | Method of making a clear personal care comprising microcapsules |
CN114981016A (en) | 2020-02-14 | 2022-08-30 | 宝洁公司 | Bottle suitable for storing liquid compositions having an aesthetic design suspended therein |
CA3074150A1 (en) | 2020-02-18 | 2021-08-18 | Ovation Science, Inc. | Composition and method for transdermal delivery of cannabidiol (cbd) and delta9-tetrahydrocannabinol (thc) |
KR102495748B1 (en) * | 2020-09-08 | 2023-02-06 | 주식회사 블리스팩 | Alcohol-based hand sanitizer of high internal phase oil-in-water emulsion type |
WO2022099149A1 (en) * | 2020-11-06 | 2022-05-12 | Aunt Fannie Inc. | Cleaning composition |
US11633072B2 (en) | 2021-02-12 | 2023-04-25 | The Procter & Gamble Company | Multi-phase shampoo composition with an aesthetic design |
WO2023059784A1 (en) | 2021-10-06 | 2023-04-13 | Lubrizol Advanced Materials, Inc. | Stabilized rheology modifier emulsions |
WO2023078870A2 (en) * | 2021-11-03 | 2023-05-11 | Firmenich Sa | Fragrance compositions with moisturizing benefits |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4990334A (en) * | 1988-11-08 | 1991-02-05 | Longino Ronald M | Glycerol-chlorine matrix |
WO1997000667A1 (en) * | 1995-06-22 | 1997-01-09 | Minnesota Mining And Manufacturing Company | Stable hydroalcoholic compositions |
Family Cites Families (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2054989A (en) | 1933-12-30 | 1936-09-22 | Us Ind Alcohol Co | Compositions for application to the human skin |
US3485915A (en) | 1966-04-22 | 1969-12-23 | Revlon | Thickened hydroxypropyl cellulose compositions |
US4014995A (en) * | 1973-09-19 | 1977-03-29 | The Quaker Oats Company | Cosmetics containing finely divided oat flour |
US4464293A (en) | 1982-04-12 | 1984-08-07 | Dobrin Robert J | Liquid cleaner-disinfectant composition for use in wiping down dental operatories |
US4970220A (en) * | 1982-05-17 | 1990-11-13 | S. C. Johnson & Son, Inc. | Skin conditioning composition |
US4446153A (en) | 1982-09-30 | 1984-05-01 | Ralston Purina Company | Skin sanitizing composition and method of using |
CA1224050A (en) | 1983-08-31 | 1987-07-14 | Peter L. Dawson | Abrasive agglomerates for use in scouring cleaning compositions |
US5288486A (en) | 1985-10-28 | 1994-02-22 | Calgon Corporation | Alcohol-based antimicrobial compositions |
US5182103A (en) * | 1985-12-09 | 1993-01-26 | Shiseido Company, Ltd. | Magnesium aluminometasilicate coated composite powder and use thereof |
US4758599A (en) | 1986-06-04 | 1988-07-19 | American Cyanamid Company | Clear, hydroalcoholic aftershave lotion which moisturizes, conditions, and prevents irritation |
JPS6320036A (en) | 1986-07-10 | 1988-01-27 | Nissan Motor Co Ltd | Production of catalyst for purifying exhaust gas |
US4800076A (en) | 1987-03-13 | 1989-01-24 | Johnson & Johnson Consumer Products, Inc. | Skin care compositions |
JPS63250311A (en) * | 1987-04-06 | 1988-10-18 | Kao Corp | Water-in-oil type cosmetic |
US5296166A (en) | 1987-04-10 | 1994-03-22 | Jerry Leong | Method of manufacturing emulsions |
JPS63313710A (en) | 1987-06-16 | 1988-12-21 | Toray Silicone Co Ltd | Face cleaning cosmetic |
US5013545A (en) | 1987-12-09 | 1991-05-07 | Thames Pharmacal Co., Inc. | Aqueous gels containing topical medicaments |
US5186857A (en) | 1988-11-14 | 1993-02-16 | Imaginative Research Associates, Inc. | Self-foaming oil compositions and process for making and using same |
JPH02140167A (en) | 1988-11-22 | 1990-05-29 | Saraya Kk | Composition for disinfecting hand and finger |
US4956170A (en) * | 1989-06-28 | 1990-09-11 | S. C. Johnson & Son, Inc. | Skin moisturizing/conditioning antimicrobial alcoholic gels |
US5162378A (en) * | 1990-04-20 | 1992-11-10 | Revlon Consumer Products Corporation | Silicone containing water-in-oil microemulsions having increased salt content |
JPH045213A (en) | 1990-04-23 | 1992-01-09 | Kao Corp | Cleansing composition |
JP3055796B2 (en) | 1990-11-19 | 2000-06-26 | 善蔵 田村 | Disinfectant composition |
US5167950A (en) * | 1991-03-28 | 1992-12-01 | S. C. Johnson & Son | High alcohol content aerosol antimicrobial mousse |
JP2780533B2 (en) | 1991-08-30 | 1998-07-30 | 株式会社ダイフク | Transport storage facilities using transport trains |
DE69208098T2 (en) * | 1991-10-16 | 1996-08-08 | Richardson Vicks Inc | AQUEOUS, COSMETIC GEL, WITH LOW PH, CONTAINING NON-IONOGENIC POLYACRYLAMIDE DERIVATIVES |
DE4140473C2 (en) | 1991-12-09 | 1995-12-21 | Schuelke & Mayr Gmbh | Skin antiseptic and hand sanitizer |
GB9200764D0 (en) | 1992-01-15 | 1992-03-11 | Unilever Plc | Cosmetic composition |
DE4205828A1 (en) | 1992-02-26 | 1993-09-02 | Henkel Kgaa | VIRUSIVE DISINFECTANT |
ES2136123T3 (en) | 1992-03-10 | 1999-11-16 | Kao Corp | SILICONE DERIVATIVE MODIFIED BY FLUORINE; PRODUCTION OF THIS DERIVATIVE AND COSMETIC CONTAINING THEM. |
US5376366A (en) | 1992-11-12 | 1994-12-27 | John Petchul | Composition and process for forming isopropyl alcohol gel with water-soluble vinyl polymer neutralizing agent |
JP2533723B2 (en) | 1992-12-28 | 1996-09-11 | 東興薬品工業株式会社 | Quick-drying gel type hand sanitizer |
US5403864A (en) | 1993-04-01 | 1995-04-04 | John A. Manfuso, Jr. | Rapidly-acting topical antimicrobial composition |
DE4320401A1 (en) | 1993-06-19 | 1994-12-22 | Wella Ag | Use of a composition in gel form as skin protective, and novel skin protectives |
US5484597A (en) | 1993-07-30 | 1996-01-16 | Chesebrough-Pond's Usa Co. | Clear hydroalcholic cosmetic microemulsions |
DE4328828A1 (en) | 1993-08-27 | 1995-03-02 | Bode Chemie Gmbh & Co | Alcoholic hand sanitizer with skin care component |
KR100344568B1 (en) | 1993-09-21 | 2002-12-28 | 가부시키가이샤 시세이도 | Disinfection Composition |
DE69412767T2 (en) | 1993-12-09 | 1999-02-11 | Kao Corp | Fluorine-modified silicone, process for its production and cosmetics containing it |
US5492932A (en) | 1994-02-22 | 1996-02-20 | Kundsin Leduc Lenmark, Inc. | Lubrication germicidal composition |
US5767163A (en) | 1994-02-22 | 1998-06-16 | Kundsin Leduc Lenmark Inc. | Lubricating and/or germicidal composition |
GB9414574D0 (en) | 1994-07-19 | 1994-09-07 | Unilever Plc | Detergent composition |
GB9414575D0 (en) | 1994-07-19 | 1994-09-07 | Unilever Plc | Detergent composition |
US5599533A (en) * | 1994-12-15 | 1997-02-04 | Estee Lauder, Inc. | Stable water-in-oil emulsion system |
US5618522A (en) | 1995-01-20 | 1997-04-08 | The Procter & Gamble Company | Emulsion compositions |
JP4497559B2 (en) | 1995-06-22 | 2010-07-07 | スリーエム カンパニー | Stable hydroalcohol composition |
KR0163512B1 (en) | 1995-12-26 | 1998-11-16 | 성재갑 | Cleansing composition of transparent gel phase |
US5750122A (en) * | 1996-01-16 | 1998-05-12 | The Procter & Gamble Company | Compositions for treating hair or skin |
US5871764A (en) | 1996-02-29 | 1999-02-16 | Johnson & Johnson Consumer Products, Inc. | Skin toning formulation |
US5654362A (en) | 1996-03-20 | 1997-08-05 | Dow Corning Corporation | Silicone oils and solvents thickened by silicone elastomers |
DE19612057A1 (en) | 1996-03-27 | 1997-10-02 | Antiseptica Chem Pharm Prod Gm | Hand disinfectant |
US5919437A (en) * | 1996-05-24 | 1999-07-06 | Colgate-Palmolive Company | Cosmetic cream composition containing silicone gel material |
US5833973A (en) | 1996-06-28 | 1998-11-10 | Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. | Crosslinked elastomeric silicones in aqueous emulsion cosmetic compositions |
US5908619A (en) | 1997-01-09 | 1999-06-01 | Minnesota Mining And Manufacturing Company | Hydroalcoholic compositions thickened using surfactant/polymer complexes |
US5747021A (en) | 1997-01-10 | 1998-05-05 | Mckenzie; Therman | After shave treatment composition |
US5854336A (en) | 1997-03-20 | 1998-12-29 | Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. | Process for preparing silicone elastomer compositions |
US5871718A (en) * | 1997-06-09 | 1999-02-16 | The Procter & Gamble Company | Perfumed two phase compositions for reducing body odor |
US5997893A (en) * | 1998-01-20 | 1999-12-07 | Ethicon, Inc. | Alcohol based anti-microbial compositions with cosmetic appearance |
-
1999
- 1999-05-27 US US09/320,997 patent/US6183766B1/en not_active Expired - Lifetime
-
2000
- 2000-02-10 DE DE60014035T patent/DE60014035D1/en not_active Expired - Lifetime
- 2000-02-10 AU AU29904/00A patent/AU2990400A/en not_active Abandoned
- 2000-02-10 EP EP00908591A patent/EP1152743B1/en not_active Expired - Lifetime
- 2000-02-10 MX MXPA01008159A patent/MXPA01008159A/en active IP Right Grant
- 2000-02-10 JP JP2000598137A patent/JP2002536398A/en active Pending
- 2000-02-10 AT AT00908591T patent/ATE276735T1/en not_active IP Right Cessation
- 2000-02-10 WO PCT/US2000/003511 patent/WO2000047184A1/en active IP Right Grant
- 2000-02-10 CN CN00804869A patent/CN1343115A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4990334A (en) * | 1988-11-08 | 1991-02-05 | Longino Ronald M | Glycerol-chlorine matrix |
WO1997000667A1 (en) * | 1995-06-22 | 1997-01-09 | Minnesota Mining And Manufacturing Company | Stable hydroalcoholic compositions |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2808443A1 (en) * | 2000-05-05 | 2001-11-09 | Nuxe Lab | MOISTURIZING COSMETIC AND / OR DERMATOLOGICAL COMPOSITION WITH IMPROVED STABILITY |
EP1151744A1 (en) * | 2000-05-05 | 2001-11-07 | Laboratoire Nuxe | Cosmetic and/or dermatologic composition with enhanced stability |
GB2369052A (en) * | 2000-09-12 | 2002-05-22 | Barrier Biotech Ltd | Antimicrobial compositions comprising a blend of essential oils |
WO2002047639A2 (en) * | 2000-12-12 | 2002-06-20 | The Procter & Gamble Company | Single-phase antiperspirant compositions containing silicone elastomer |
WO2002047639A3 (en) * | 2000-12-12 | 2003-01-09 | Procter & Gamble | Single-phase antiperspirant compositions containing silicone elastomer |
US6524562B2 (en) | 2000-12-12 | 2003-02-25 | The Procter & Gamble Company | Single-phase antiperspirant compositions containing solubilized antiperspirant active and silicone elastomer |
WO2002051379A2 (en) * | 2000-12-23 | 2002-07-04 | Impetus Ag | Thixotropic nasal spray |
WO2002051379A3 (en) * | 2000-12-23 | 2003-03-13 | Impetus Ag | Thixotropic nasal spray |
DE10296678B4 (en) * | 2001-04-18 | 2014-03-27 | Kimberly-Clark Worldwide, Inc. | Anionic carboxymethylcellulose particle-containing skin cleansing composition |
DE10226349A1 (en) * | 2002-06-13 | 2003-12-24 | Beiersdorf Ag | Cosmetic and dermatological light protection preparations containing a combination of UV absorbers and spherical silicon oxides |
CN102885697A (en) * | 2011-07-22 | 2013-01-23 | 陈进民 | Inflammation diminishing and sterilizing flower perfume and preparation method thereof |
US9717669B2 (en) | 2012-07-23 | 2017-08-01 | Innovative Biodefense, Inc. | Topical sanitizing formulations and uses thereof |
EP3206487B1 (en) | 2014-10-16 | 2021-12-29 | Schülke & Mayr GmbH | Use of fatty acid ester for improving the antimicrobial efficacy of an alcoholic disinfectant |
RU2769876C1 (en) * | 2018-10-31 | 2022-04-07 | ЮНИЛЕВЕР АйПи ХОЛДИНГС Б. В. | Antimicrobial composition |
WO2020126347A1 (en) * | 2018-12-18 | 2020-06-25 | Unilever N.V. | An antimicrobial composition |
DE102018133179A1 (en) * | 2018-12-20 | 2020-06-25 | Brauns-Heitmann Gmbh & Co Kg | Disinfectant composition |
WO2021219622A1 (en) * | 2020-04-30 | 2021-11-04 | Dsm Ip Assets B.V. | Hand sanitiser composition |
Also Published As
Publication number | Publication date |
---|---|
MXPA01008159A (en) | 2002-04-24 |
EP1152743A1 (en) | 2001-11-14 |
AU2990400A (en) | 2000-08-29 |
JP2002536398A (en) | 2002-10-29 |
ATE276735T1 (en) | 2004-10-15 |
EP1152743B1 (en) | 2004-09-22 |
US6183766B1 (en) | 2001-02-06 |
DE60014035D1 (en) | 2004-10-28 |
CN1343115A (en) | 2002-04-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1152743B1 (en) | Skin sanitizing compositions | |
US6423329B1 (en) | Skin sanitizing compositions | |
EP1152744B1 (en) | Skin sanitizing compositions | |
EP1043942B2 (en) | Soft tissue achieved by applying a solid hydrophilic lotion | |
KR20020042729A (en) | Antimicrobial compositions comprising pyroglutamic acid and optionally metal salts | |
CA2387348A1 (en) | Antimicrobial compositions comprising a benzoic acid analog and a metal salt | |
JP2001506275A (en) | Perfume-free two-phase composition and method for reducing body odor and external odor | |
JP2010530456A (en) | Stable high internal phase emulsion and composition thereof | |
MXPA06014074A (en) | Antimicrobial tissue products with reduced skin irritation potential. | |
US20160354289A1 (en) | Antimicrobial Anti-Chafing Chelated Silver Oxide Compound | |
CN101321561A (en) | Water in oil emulsion compositions containing siloxane elastomers | |
JP3250858B2 (en) | Keratin fiber treatment composition | |
WO2010063988A1 (en) | Germicidal topical compositions | |
GB2422605A (en) | Ionic thickening agent for compositions | |
US9844596B2 (en) | Compositions for depositing agents using highly volatile silicone solvents | |
EP2068818B1 (en) | Cosmetic compositions with ethylene brassylate | |
KR102495748B1 (en) | Alcohol-based hand sanitizer of high internal phase oil-in-water emulsion type | |
CN116600642A (en) | Sterile, skin-tolerant, care and moisturizing formulation for application to skin | |
JP2022045971A (en) | Oil-in-water type emulsion composition | |
NZ708493A (en) | Compositions for depositing agents using highly volatile silicone solvents | |
NZ708493B2 (en) | Compositions for depositing agents using highly volatile silicone solvents |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 00804869.X Country of ref document: CN |
|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AL AM AT AT AU AZ BA BB BG BR BY CA CH CN CR CU CZ CZ DE DE DK DK DM EE EE ES FI FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SK SL TJ TM TR TT TZ UA UG UZ VN YU ZA ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): GH GM KE LS MW SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
WWE | Wipo information: entry into national phase |
Ref document number: PA/a/2001/008159 Country of ref document: MX |
|
ENP | Entry into the national phase |
Ref document number: 2000 598137 Country of ref document: JP Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2000908591 Country of ref document: EP |
|
WWP | Wipo information: published in national office |
Ref document number: 2000908591 Country of ref document: EP |
|
REG | Reference to national code |
Ref country code: DE Ref legal event code: 8642 |
|
WWG | Wipo information: grant in national office |
Ref document number: 2000908591 Country of ref document: EP |