USRE33845E - Novel skin tanning composition - Google Patents
Novel skin tanning composition Download PDFInfo
- Publication number
- USRE33845E USRE33845E US07/630,822 US63082290A USRE33845E US RE33845 E USRE33845 E US RE33845E US 63082290 A US63082290 A US 63082290A US RE33845 E USRE33845 E US RE33845E
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- 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
- A61Q19/04—Preparations for care of the skin for chemically tanning 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
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
Definitions
- compositions have been proposed for skin tanning over the course of the years. Some of these proposed compositions contain as active main ingredient panthenol which is applied in an acid, non aqueous phase, and are indeed effecting the desired skin tanning after exposure to natural or artificial sunlight.
- panthenol which is applied in an acid, non aqueous phase
- the action is too slow.
- compounds which have to protect the skin temporarily against excessive interaction of harmful frequencies in the light spectrum, leading to burning before the actual skin tanning process due to the natural production of melanoprotein (pigment) has taken place in a sufficient degree have to be incorporated into these skin tanning agents.
- These so called light filtering agents are still regarded undesirable due to a possible disturbence of the biological equilibrium of the skin and the toxicity of these compounds for humans in large concentrations due to accumulation.
- novel sun tanning compositions of the invention are comprised of (a) 5 to 50% by weight of an oil fraction of straight or branched paraffinic oils of 10 to 30 carbon atoms with a boiling range of 100° to 500° C. at atmospheric pressure and a viscosity of at most 35 centistokes at 25° C.
- emulsifying system comprising (1) 1 to 10% by weight of mono and/or diglycerides of higher optionally unsaturated natural fatty acids and (2) ethoxylated glycerides esterified with fatty acids of the formula ##STR2## wherein n is an integer from 5 to 20 and the R's are individually an optionally unsaturated fatty acid residue derived from animal or vegetable oils with a ratio of 10 to 100 parts by weight of (1) per part of weight of (2), (c) .[.1.0 to 5% by weight of a mixture.].
- the oil fraction consists of straight or branched parrafinic oils containing 10 to 30 carbon atoms in the chain and preferably 12 to 25 carbon atoms in an amount of 5 to 50% by weight and preferably from 10 to 40% by weight, calculated on the weight of the total system.
- paraffinic oils have a boiling range of from 100° to 500° C. at atmospheric pressure and show a viscosity of at most 35 centistokes at 25° C.
- the paraffinic oils may be optionally mixed with esters of optionally unsaturated higher natural fatty acids and of higher natural aliphatic alcohols of up to 20 carbon atoms in the chain such as oleyl oleate or oleyl decalate (e.g. Cetiol V®.
- esters of optionally unsaturated higher natural fatty acids and of higher natural aliphatic alcohols of up to 20 carbon atoms in the chain such as oleyl oleate or oleyl decalate (e.g. Cetiol V®.
- the terms "higher natural fatty acids” and “higher natural alcohols” mean fatty acids and alcohols which maybe derived from products occurring in nature such as animal or vegetable oils and fats such as linseed oil, sunflower oil, rape oil, whale oil, castor oil, peanut oil, palm oil, olive oil, coconut oil, soybean oil, tung oil. It appears that for the most effective compositions, these esters are added to the paraffinic oil fractions in an
- the emulsifying system mainly consists of (a) mono and/or diglycerides of higher unsaturated and/or saturated natural fatty acids such as linoleic acid, oleic acid, linolenic acid, eleostearic acid, palmitic acid, lauric acid, or mixtures thereof (e.g.
- Tegomuls® in an amount of 1 to 10% by weight and preferably 2 to 8% by weight, calculated on the weight of the complete composition, and (b) ethoxylated glycerides derived from fatty acids of the formula ##STR3## wherein n is a number from 5 to 20 and preferably from 7 to 15 and R is a saturated or unsaturated and preferably unsaturated fatty acid residue derived from vegetable or animal oils, while R may be same or different fatty acid residues in one molecule, but preferably the same (e.g. Tagat TO®.
- the emulsifying system only will have to be used in relatively small amounts of the decidedly indispensable, but with reference to skin affections undesired emulsifier, whereas on the other hand the present emulsifying system may be regarded as especially affable to the skin, which feature is connected with a relatively low hydrophilic-lipophylic balance value.
- the ratio between the amount of the mono and diglycerides and the ethoxylated triglycerides may vary, whereas the advantageous characteristics are maintained, from 10 to 100 parts of mono and diglycerides per part of ethoxylated triglycerides and preferably 25 parts of mono and/or diglycerides per part of ethoxylated triglycerides.
- the total amount of the emulsifying system, calculated on the weight of the total composition may vary from 1 to 10% by weight and preferably 2 to 8% by weight, for the most optimal results.
- the stabilizer consists of montmorillonites whose free oxygen sites are occupied by quaternary groups (quaternary modified montmorillonites).
- quaternary modified montmorillonites examples of such stabilizers which are preferably employed are Bentone® or Propoloid® preparations which are added in an amount of from 0.2 to 4% by weight and preferably 0.5 to 2% by weight, calculated on the weight of the total composition.
- Panthenol may be used in one of its pure optical isomeric forms or as a racemic mixture, but preferably as D-panthenol, and tyrosine in one of its pure optical isomer forms or as racemic mixture, but preferably as L-tyrosine, or a compound from which the tyrosine easily may be formed in situ such as e.g. esters of tyrosine or phenylalanine which are known to be readily soluble in the aqueous phase. It will be appreciated that it is generally known that phenylalanine can be easily converted into tyrosine under natural conditions.
- Tyrosine is preferably added in the form of lower alkyl esters such as methyl, ethyl, (iso)propyl or (iso)butyl ester or in the form of the stearyl ester or the benzyl ester wherein the amino group optionally may be temporarily protected in a known way and is preferably protected by HCl addition.
- the aqueous phase wherein the panthenol and the tyrosine ester ultimately have to be present may have a pH in the range of 4 to 7 and more preferably in the range of 4 to 6 which may be obtained by addition of suitable alkaline agent such as sodium citrate and/or sodium hydroxide, especially in the case of protection of the amino group by HCl addition.
- suitable alkaline agent such as sodium citrate and/or sodium hydroxide
- the amounts of e.g. sodium citrate and/or sodium hydroxide will vary, depending on the specific protecting groups in the starting tyrosine derivative from 0.1 to 3% by weight, calculated on the weight of the complete composition.
- the molar ratio of tyrosine and panthenol should be in the range from 2:1 to 1:3 reach the indicated attractive properties of the compositions of the invention while the amounts of panthenol and tyrosine or tyrosine providing means should be 1 to 5% by weight (and preferably 2 to 4% by weight) and 0.5 to 5% by weight (preferably 1 to 4% by weight) respectively, calculated on the weight of the complete composition.
- the preservative is preferably selected from different types of preservatives which can be used for the ultimately formed continuous oily phase and the dispersed aqueous phase.
- esters of p-hydroxy benzoic acid are used for the oily phase and preferably the methyl and/or the (iso)propyl ester and/or (iso)butyl ester is used in an amount of 0.05 to 1% by weight, calculated on the weight of the complete composition, and preferably in an amount of 0.2 to 0.4% by weight.
- Preferred are mixtures of methyl, propyl and butyl-p-hydroxy-benzoate (e.g. Phenonip®.
- preservatives may be completely or partially replaced by other preservatives (e.g. Germall 115® or Hydroconserv® in an amount of 0.05 to 1% by weight and preferably 0.2 to 0.4% by weight in the dispersed aqueous phase.
- other preservatives e.g. Germall 115® or Hydroconserv® in an amount of 0.05 to 1% by weight and preferably 0.2 to 0.4% by weight in the dispersed aqueous phase.
- one or more secondary ingredients also can be added to the final composition if desired, such as: (a) vitamin E as such or preferably in the relatively stable acetate form in an amount of 0.05 to 5% by weight calculated on the weight of the complete composition and preferably in an amount of from 0.2 to 2% by weight. (b) glycerol in an amount of 0.5 to 5.0% by weight, calculated on the weight of the complete composition and preferably in an amount of from 1 to 3% by weight, to form a moisture regulating system, together with the panthenol and optionally co-added sodium lactate and/or possibly alkali to maintain the desired pH of from 4 to 7 such as sodium citrate.
- vitamin E as such or preferably in the relatively stable acetate form in an amount of 0.05 to 5% by weight calculated on the weight of the complete composition and preferably in an amount of from 0.2 to 2% by weight.
- glycerol in an amount of 0.5 to 5.0% by weight, calculated on the weight of the complete composition and preferably in an amount of from 1
- alkali such as sodium citrate, sodium hydroxide and optional sodium lactate will vary from 0.1 to 5% by weight.
- a gelforming agents such as carraghenate, preferably consisting of a polysaccharide bearing sulfonic acid residues, and preferably those of natural origin such as those derived from seaweed. The sulfonic acid residues have optionally been converted into salts or esters of glycol, propylene glycol and glycerol (the so called modified carraghenates).
- the beforementioned carraghenates cause a gel structure in the final complete composition in the amounts of from 0.1 to 5% by weight, calculated on the weight of the complete composition, and preferably 0.5 to 2% by weight.
- a complete composition shows a viscosity of 200 to 5000 centipoises at 25° C., which is desired for an adequate application of the composition.
- the carraghenate may be completely or partially replaced by alternative gel forming means, such as carboxy methyl cellulose, esterified by polyacrylic acid (e.g. Carbopol® or hydroxy ethyl cellulose, in amounts which lead to viscosity values situated in the beforementioned range.
- perfume in an amount of from 0.1 to 0.5% by weight, calculated on the weight of the complete composition .
- anti oxidants in an amount of from 0.01 to 3% by weight, calculated on the weight of the complete composition.
- an alkanol and more preferably ethanol (96%) in an amount of from 0.1 to 1.0% by weight and preferably 0.3 to 0.6% by weight, calculated on the weight of the complete composition.
- the alkanol may be added to reach a fat gelation of the quaternary modified montmorillonites.
- compositions of the invention are characterized by a relatively low viscosity and high stability which guarantees an easy application without a "greasy” feeling or stickiness and stains in clothes due to a fast penetration into the skin tissue, and they give the skin the desired tanning by means of natural pigment formation in the skin after a relatively short period of exposure to light.
- compositions of the invention may be prepared by a process which should be regarded as another aspect of the invention which is characterized by a specific sequence of addition and the dosing rate of the respective beforementioned ingredients and by the temperature and stirring speeds at which this addition c.q. dosing takes place.
- the first step of the process comprises the preparation of the complete continuous oily phase composed of the oil fractions, the esters of the unsaturated fatty acids and alcohols, emulsifying system, stabilizers, preservatives and alkanol, e.g. ethanol while the dispersed aqueous phase is composed of water, glycerol, panthenol, tyrosine or tyrosine providing compound, desired alkali and carraghenate. Vitamin E and the possible perfume may be added to the prepared emulsion.
- compositions of the invention are preferably preferred by mixing both phases together at a temperature of at most 30° C., followed by additional stirring after the possible addition of Vitamin E and perfume until an average particle size of the dispersed aqueous phase is at most 5 ⁇ , and preferably smaller than 3 ⁇ .
- compositions i.e. the treatment of the skin with the before described compositions
- Such an application comprises a method usual for such compositions characterized by application and spreading evenly onto the skin area involved of an amount of 20 to 100 ml/m 2 skin area, if necessary after thorough cleaning of the skin with water and soap or an alcoholic solution, preceeding the exposure of the skin to natural or artificial sunlight.
- This treatment should be preferably be repeated 2 to 3 times a day.
- the aqueous phase was prepared by dissolving the following ingredients in 687 g of water
- the resulting aqueous phase was then mixed with the oily phase and homogenized after addition of 10 g of vitamin E-acetate (D-isomer) and 2 g of perfume.
- the water-in-oil emulsion was further homogenized until an average particle size ⁇ 3 ⁇ was reached.
- Example 2 Using the procedure of Example 1, a composition was prepared from the following ingredients:
- Example 2 Using the procedure of Example 1, a composition was prepared from the following ingredients:
- composition was prepared from the following ingredients:
- Example 2 Using the procedure of Example 1, a composition was prepared from the following ingredients:
- compositions caused a fast, intensive natural skin tanning within some hours of exposure after the application in the usual way.
Abstract
Skin tanning composition, comprising at least the following ingredients: - an oil fraction, comprising straight or branched paraffinic oils, having 10-30 carbon atoms in the chain and preferably 15-25 carbon atoms, - an emulsifying systen, mainly comprising: a) mono and/or diglycerides of higher unsaturated and/or saturated natural fatty acids, and b) ethoxylated glycerides, esterified with fatty acids, whereby the ratio between the amount of mono and/or diglycerides on the one hand and of the ethoxylated triglycerides on the other hand may vary from 10-100 parts mono and/or diglycerides pro part ethoxylated triglycerides, - panthenol and more preferably D-panthenol, and tyrosine and more preferably L-tyrosine, or a compound from which tyrosine may be easily formed in situ in the aqueous phase, the pH of which has to be in the range from 4-7, in a mutual molar ratio of tyrosine : panthenol between 2:1 and 1:3, - alkali to adjust the pH of the aqueous phase to be in the range from 4-7, e.g. in the form of sodium citrate and/or sodium hydroxide. - a stabilizer, consisting of montmorillonites, the free oxygen sites of which are occupied by quaternary groups, - a preservative, being the same or different for the formed contineous oily phase and the dispersed aqueous phase, - water ad 100 % by weight.
Description
This application is a continuation of U.S. patent application Ser. No. 344,203 filed Apr. 27, 1989, now abandoned which is a reissue of Ser. No. 064,331, filed Jun. 19, 1987, now U.S. Pat. No. 4,783,332.
Many compositions have been proposed for skin tanning over the course of the years. Some of these proposed compositions contain as active main ingredient panthenol which is applied in an acid, non aqueous phase, and are indeed effecting the desired skin tanning after exposure to natural or artificial sunlight. However, in the opinion of the modern consumer, the action is too slow. For this reason, compounds which have to protect the skin temporarily against excessive interaction of harmful frequencies in the light spectrum, leading to burning before the actual skin tanning process due to the natural production of melanoprotein (pigment) has taken place in a sufficient degree, have to be incorporated into these skin tanning agents. These so called light filtering agents are still regarded undesirable due to a possible disturbence of the biological equilibrium of the skin and the toxicity of these compounds for humans in large concentrations due to accumulation.
It is an object of the invention to provide novel tanning compositions containing harmless, fast acting skin tanning agents, wherein the light filtering agents do not need to be used.
It is another object of the invention to provide an improved method of fast tanning of skin.
These and other objects and advantages of the invention will become obvious from the following detailed description.
The novel sun tanning compositions of the invention are comprised of (a) 5 to 50% by weight of an oil fraction of straight or branched paraffinic oils of 10 to 30 carbon atoms with a boiling range of 100° to 500° C. at atmospheric pressure and a viscosity of at most 35 centistokes at 25° C. optionally containing up to 6% by weight of esters of optionally unsaturated higher natural fatty acids and optionally unsaturated natural aliphatic alcohols of up to 20 carbon atoms, (b) 1 to 10% by weight of an emulsifying system comprising (1) 1 to 10% by weight of mono and/or diglycerides of higher optionally unsaturated natural fatty acids and (2) ethoxylated glycerides esterified with fatty acids of the formula ##STR2## wherein n is an integer from 5 to 20 and the R's are individually an optionally unsaturated fatty acid residue derived from animal or vegetable oils with a ratio of 10 to 100 parts by weight of (1) per part of weight of (2), (c) .[.1.0 to 5% by weight of a mixture.]. .Iadd.1 to 5% by weight of panthenol and 0.5 to 5% by weight of tyrosine or tyrosine precursor in a molar ratio .Iaddend.of 2:1 to 1:3 of tyrosine or tyrosine precursor to panthenol, (d) sufficient alkali to maintain the pH of the aqueous phase at 4 to 7, (e) 0.2 to 4% by weight of a montmorillonite stabilizer with free oxygen sites occupied by quaternary groups, (f) 0.05 to 1.0% by weight of a preservative for the formed continuous oily phase and the dispersed aqueous phase and (g) water to make up 100% by weight, the weights being based on the weight of the entire composition.
Preferably, the oil fraction consists of straight or branched parrafinic oils containing 10 to 30 carbon atoms in the chain and preferably 12 to 25 carbon atoms in an amount of 5 to 50% by weight and preferably from 10 to 40% by weight, calculated on the weight of the total system. These paraffinic oils have a boiling range of from 100° to 500° C. at atmospheric pressure and show a viscosity of at most 35 centistokes at 25° C.
The paraffinic oils may be optionally mixed with esters of optionally unsaturated higher natural fatty acids and of higher natural aliphatic alcohols of up to 20 carbon atoms in the chain such as oleyl oleate or oleyl decalate (e.g. Cetiol V®. The terms "higher natural fatty acids" and "higher natural alcohols" mean fatty acids and alcohols which maybe derived from products occurring in nature such as animal or vegetable oils and fats such as linseed oil, sunflower oil, rape oil, whale oil, castor oil, peanut oil, palm oil, olive oil, coconut oil, soybean oil, tung oil. It appears that for the most effective compositions, these esters are added to the paraffinic oil fractions in an amount up to 6% by weight and preferably 2 to 5% by weight, based on the weight of the total composition.
The emulsifying system mainly consists of (a) mono and/or diglycerides of higher unsaturated and/or saturated natural fatty acids such as linoleic acid, oleic acid, linolenic acid, eleostearic acid, palmitic acid, lauric acid, or mixtures thereof (e.g. Tegomuls® in an amount of 1 to 10% by weight and preferably 2 to 8% by weight, calculated on the weight of the complete composition, and (b) ethoxylated glycerides derived from fatty acids of the formula ##STR3## wherein n is a number from 5 to 20 and preferably from 7 to 15 and R is a saturated or unsaturated and preferably unsaturated fatty acid residue derived from vegetable or animal oils, while R may be same or different fatty acid residues in one molecule, but preferably the same (e.g. Tagat TO®.
It will be appreciated that the emulsifying system only will have to be used in relatively small amounts of the decidedly indispensable, but with reference to skin affections undesired emulsifier, whereas on the other hand the present emulsifying system may be regarded as especially affable to the skin, which feature is connected with a relatively low hydrophilic-lipophylic balance value. The ratio between the amount of the mono and diglycerides and the ethoxylated triglycerides may vary, whereas the advantageous characteristics are maintained, from 10 to 100 parts of mono and diglycerides per part of ethoxylated triglycerides and preferably 25 parts of mono and/or diglycerides per part of ethoxylated triglycerides. The total amount of the emulsifying system, calculated on the weight of the total composition, may vary from 1 to 10% by weight and preferably 2 to 8% by weight, for the most optimal results.
The stabilizer consists of montmorillonites whose free oxygen sites are occupied by quaternary groups (quaternary modified montmorillonites). Examples of such stabilizers which are preferably employed are Bentone® or Propoloid® preparations which are added in an amount of from 0.2 to 4% by weight and preferably 0.5 to 2% by weight, calculated on the weight of the total composition. By addition of the said stabilizers, deposit of one or more of the ingredients of the compositions is avoided in the relatively low viscous compositions which are preferred for practical reasons.
Panthenol (provitamin B-5) may be used in one of its pure optical isomeric forms or as a racemic mixture, but preferably as D-panthenol, and tyrosine in one of its pure optical isomer forms or as racemic mixture, but preferably as L-tyrosine, or a compound from which the tyrosine easily may be formed in situ such as e.g. esters of tyrosine or phenylalanine which are known to be readily soluble in the aqueous phase. It will be appreciated that it is generally known that phenylalanine can be easily converted into tyrosine under natural conditions.
With regard to the known poor solubility of tyrosine as such in an aqueous phase, the good properties of the present compositions could certainly not be expected or predicted by people skilled in the art. Tyrosine is preferably added in the form of lower alkyl esters such as methyl, ethyl, (iso)propyl or (iso)butyl ester or in the form of the stearyl ester or the benzyl ester wherein the amino group optionally may be temporarily protected in a known way and is preferably protected by HCl addition.
Additionally, it was found that the aqueous phase wherein the panthenol and the tyrosine ester ultimately have to be present may have a pH in the range of 4 to 7 and more preferably in the range of 4 to 6 which may be obtained by addition of suitable alkaline agent such as sodium citrate and/or sodium hydroxide, especially in the case of protection of the amino group by HCl addition. The amounts of e.g. sodium citrate and/or sodium hydroxide will vary, depending on the specific protecting groups in the starting tyrosine derivative from 0.1 to 3% by weight, calculated on the weight of the complete composition.
The molar ratio of tyrosine and panthenol should be in the range from 2:1 to 1:3 reach the indicated attractive properties of the compositions of the invention while the amounts of panthenol and tyrosine or tyrosine providing means should be 1 to 5% by weight (and preferably 2 to 4% by weight) and 0.5 to 5% by weight (preferably 1 to 4% by weight) respectively, calculated on the weight of the complete composition.
The preservative is preferably selected from different types of preservatives which can be used for the ultimately formed continuous oily phase and the dispersed aqueous phase. For example, esters of p-hydroxy benzoic acid are used for the oily phase and preferably the methyl and/or the (iso)propyl ester and/or (iso)butyl ester is used in an amount of 0.05 to 1% by weight, calculated on the weight of the complete composition, and preferably in an amount of 0.2 to 0.4% by weight. Preferred are mixtures of methyl, propyl and butyl-p-hydroxy-benzoate (e.g. Phenonip®. It will be appreciated that the said preservatives may be completely or partially replaced by other preservatives (e.g. Germall 115® or Hydroconserv® in an amount of 0.05 to 1% by weight and preferably 0.2 to 0.4% by weight in the dispersed aqueous phase.
In addition to the beforementioned primary indispensable ingredients, one or more secondary ingredients also can be added to the final composition if desired, such as: (a) vitamin E as such or preferably in the relatively stable acetate form in an amount of 0.05 to 5% by weight calculated on the weight of the complete composition and preferably in an amount of from 0.2 to 2% by weight. (b) glycerol in an amount of 0.5 to 5.0% by weight, calculated on the weight of the complete composition and preferably in an amount of from 1 to 3% by weight, to form a moisture regulating system, together with the panthenol and optionally co-added sodium lactate and/or possibly alkali to maintain the desired pH of from 4 to 7 such as sodium citrate. The total amount of alkali such as sodium citrate, sodium hydroxide and optional sodium lactate will vary from 0.1 to 5% by weight. (c) a gelforming agents such as carraghenate, preferably consisting of a polysaccharide bearing sulfonic acid residues, and preferably those of natural origin such as those derived from seaweed. The sulfonic acid residues have optionally been converted into salts or esters of glycol, propylene glycol and glycerol (the so called modified carraghenates).
The beforementioned carraghenates cause a gel structure in the final complete composition in the amounts of from 0.1 to 5% by weight, calculated on the weight of the complete composition, and preferably 0.5 to 2% by weight. Such a complete composition shows a viscosity of 200 to 5000 centipoises at 25° C., which is desired for an adequate application of the composition. It will be appreciated by a person skilled in this specific art, that the carraghenate may be completely or partially replaced by alternative gel forming means, such as carboxy methyl cellulose, esterified by polyacrylic acid (e.g. Carbopol® or hydroxy ethyl cellulose, in amounts which lead to viscosity values situated in the beforementioned range.
Also useful are (d) perfume, in an amount of from 0.1 to 0.5% by weight, calculated on the weight of the complete composition . (e) anti oxidants in an amount of from 0.01 to 3% by weight, calculated on the weight of the complete composition. (f) an alkanol, and more preferably ethanol (96%) in an amount of from 0.1 to 1.0% by weight and preferably 0.3 to 0.6% by weight, calculated on the weight of the complete composition. The alkanol may be added to reach a fat gelation of the quaternary modified montmorillonites.
The compositions of the invention are characterized by a relatively low viscosity and high stability which guarantees an easy application without a "greasy" feeling or stickiness and stains in clothes due to a fast penetration into the skin tissue, and they give the skin the desired tanning by means of natural pigment formation in the skin after a relatively short period of exposure to light.
The compositions of the invention may be prepared by a process which should be regarded as another aspect of the invention which is characterized by a specific sequence of addition and the dosing rate of the respective beforementioned ingredients and by the temperature and stirring speeds at which this addition c.q. dosing takes place.
The first step of the process comprises the preparation of the complete continuous oily phase composed of the oil fractions, the esters of the unsaturated fatty acids and alcohols, emulsifying system, stabilizers, preservatives and alkanol, e.g. ethanol while the dispersed aqueous phase is composed of water, glycerol, panthenol, tyrosine or tyrosine providing compound, desired alkali and carraghenate. Vitamin E and the possible perfume may be added to the prepared emulsion.
The compositions of the invention are preferably preferred by mixing both phases together at a temperature of at most 30° C., followed by additional stirring after the possible addition of Vitamin E and perfume until an average particle size of the dispersed aqueous phase is at most 5μ, and preferably smaller than 3μ.
It will be appreciated by a person skilled in the art that the application of the said compositions, i.e. the treatment of the skin with the before described compositions, forms another aspect of the invention. Such an application comprises a method usual for such compositions characterized by application and spreading evenly onto the skin area involved of an amount of 20 to 100 ml/m2 skin area, if necessary after thorough cleaning of the skin with water and soap or an alcoholic solution, preceeding the exposure of the skin to natural or artificial sunlight. This treatment should be preferably be repeated 2 to 3 times a day.
In the following examples there are described several preferred embodiments to illustrate the invention. However, it should be understood that the invention is not intended to be limited to the specific embodiments.
______________________________________
Paraffinic oil I 130 g
(Shell Ondina 15 ®, boiling range 295 to
390° C.)
Paraffinic oil II 30 g
(Shell Ondina 68 ®, boiling range 290 to
500° C.)
Mono and/or diglycerides (Tegomuls ®)
25 g oily
Oleyl decalate (Cetiol V ®)
30 g phase
Ethoxylated triglycerides (Tagat TO ®)
1 g
Preservatives I (Phenonip ®)
2 g
followed by addition of quaternary modified
6 g
montmorillonites (Bentone 38 ®)
and gelation by addition of 96% ethanol
3 g
______________________________________
The aqueous phase was prepared by dissolving the following ingredients in 687 g of water
______________________________________
Glycerol 20 g
Phenyl alanine 20 g
Sodium citrate 10 g aqueous
D-panthenol 16 g phase
Preservative II (Hydroconserv ®)
3 g
Carraghenate 5 g
______________________________________
The resulting aqueous phase was then mixed with the oily phase and homogenized after addition of 10 g of vitamin E-acetate (D-isomer) and 2 g of perfume. The water-in-oil emulsion was further homogenized until an average particle size <3 μwas reached.
Using the procedure of Example 1, a composition was prepared from the following ingredients:
______________________________________
Paraffinic oil I 250 g
Paraffinic oil II 50 g
Mono and/or diglycerides
40 g
Ethoxylated triglycerides
2 g oily
Preservative I 2 g phase
Quaternary modified montmorillonites
6 g
(Bentone 27 ®)
Ethanol 3 g
and
Water 580 g
Glycerol 15 g
L-tyrosine ethylate HCl
10 g
Sodium Hydroxide 1 g aqueous
D-panthenol 10 g phase
Sodium lactate 10 g
Preservative I 3 g
Carraghenate 8 g
and
Vitamin E-acetate (D-isomer)
8 g
Perfume 2 g
______________________________________
Using the procedure of Example 1, a composition was prepared from the following ingredients:
______________________________________
Paraffinic oil I 150 g
Paraffinic oil II 40 g
Mono and/or diglycerides
30 g
Ethoxylated triglycerides
1 g
Oleyl oleate 20 g oily phase
Preservative I 2 g
Quaternary modified
montmorillonites (Bentone 38 ®)
6 g
Ethanol 2 g
and
Water 659 g
Glycerol 15 g
L-tyrosine isobutylate
30 g aqueous -Sodium citrate 10 g phase
D-panthenol 20 g
Preservative III (Euxyl 100 ®)
3 g
and
Vitamin E-acetate (D-isomer)
10 g
Perfume 2 g
______________________________________
Using the procedure of Example 1, composition was prepared from the following ingredients:
______________________________________
Paraffinic oil I 140 g
Paraffinic oil II 25 g
Mono and/or diglycerides
15 g
Oleyl decalate 26 g
Ethoxylated triglycerides
0.5 g oily phase
Preservative I 3 g
Quaternary modified 7 g
montmorillonites (Bentone 27 ®)
Ethanol 3 g
and
Water 692.5 g
Glycerol 20 g
L-tyrosine ethylate HCl
15 g
Sodium hydroxide 10 g
D-panthenol 15 g aqueous
Sodium lactate 4 g phase
Sodium citrate 3 g
Preservative I 3 g
Carraghenate 8 g
and
Vitamin E-acetate (D-isomer)
7 g
Perfume 3 g
______________________________________
Using the procedure of Example 1, a composition was prepared from the following ingredients:
______________________________________
Paraffinic oil I 200 g
Paraffinic oil II 50 g
Mono and/or diglycerides
40 g
Ethoxylated triglycerides
2 g oily
Preservative I 2 g phase
Quaternary modified 6 g
montmorillonites (Benton 2 ®)
Isopropanol 2 g
and
Water 613 g
Glycerol 15 g
D,L-tyrosine isobutylate
25 g aqueous
D,L-Panthenol 20 g phase
Sodium citrate 10 g
Preservative III 3 g
Vitamin E-acetate (D,L)
10 g
Perfume 2 g
______________________________________
The said compositions caused a fast, intensive natural skin tanning within some hours of exposure after the application in the usual way.
Various modifications of the compositions and methods of the invention may be made without departing from the spirit or scope thereof and it is to be understood that the invention is intended to be limited only as defined in the appended claims.
Claims (10)
1. A skin tanning composition comprising (a) 5 to 50% by weight of an oil fraction of straight or branched paraffinic oils of 10 to 30 carbon atoms with a boiling range of 100° to 500° C. at atmospheric pressure and a viscosity of at most 35 centistokes at 25° C., containing 0 to 6% by weight of esters of saturated or unsaturated higher natural fatty acids and saturated or unsaturated natural aliphatic alcohols of up to 20 carbon atoms, (b) 1 to 10% by weight of of an emulsifying system comprising (1) to 10% by weight mono and/or diglycerides of higher saturated or unsaturated natural fatty acids and (2) ethoxylated glycerides esterified with fatty acids of the formula ##STR4## wherein n is an integer from 5 to 20 and the R's are individually a saturated or unsaturated fatty acid residue derived from animal or vegetable oils with a ratio of 10 to 100 parts by weight of (1) per part by weight of (2), (c) .[.1.0 to 5% by weight of a mixture.]..Iadd.1 to 5% by weight of panthenol and 0.5 to 5% by weight of tyrosine or tyrosine precursor in a molar ratio .Iaddend.of 2:1 to 1:3 of tyrosine or tyrosine precursor to panthenol, (d) sufficient alkali to maintain the pH of the aqueous phase at 4 to 7, (e) 0.2 4% by weight of a montmorillonite stabilizer with free oxygen sites occupied by quaternary groups, (f) 0.05 to 1.0% by weight of a preservative for the formed continuous oily phase and the dispersed aqueous phase and (g) water to make up 100% by weight, the weights being based on the weight of the entire composition.
2. A composition of claim 1 wherein (a) the paraffinic oils have 15 to 25 carbon atoms and the oil fraction is 10 to 40% by weight of the composition, (b) η is an integer from 7 to 15, (c) the panthenol is D-panthenol .Iadd.in an amount of 2 to 4% by weight and the tyrosine is L-tyrosine and the amount .[.of each of those components is 0.5 to 5%.]. .Iadd.is 1 to 4%by weight, .Iaddend.(d) the pH is 4 to 6 and the alkaline agent is sodium citrate and/or sodium hydroxide.
3. A composition of claim 1 wherein it further contains at least one ingredient selected from the group consisting of vitamin E is an amount of 0.05 to 5% by weight, glycerol in an amount of 0.5 to 5.0% by weight, alkanol in an amount of 0.1 to 1.0% by weight, sodium lactate in an amount of 0.1 to 5% by weight, gel forming agent in an amount of 0.1 to 5% by weight, perfume in an amount of 0.1 to 0.5% by weight and antioxidants in an amount of 0.01 to 3% by weight, calculated on the weight of the complete composition.
4. A composition of claim 1 wherein it contains an oil fraction in an amount of 10 to 40% by weight.
5. A composition of claim 1 wherein the oil fraction is mixed with oleyl oleate or oleyl decalate in an amount of 2 to 5% by weight, calculated on the weight of the complete composition.
6. A composition of claim 1 wherein the emulsifying system is composed of ethoxylated triglycerides derived from linoleic acid, oleic acid, linolenic acid or mixtures thereof mixed with mono and/or diglycerides derived from linoleic acid, linolenic acid, oleic acid, palmitic acid, lauric acid, myristic acid, stearic acid, eleostearic acid and mixtures thereof.
7. A composition of claim 1 wherein the ratio between mono and/or diglycerides and ethoxylated triglycerides is 25 parts mono and/or diglycerides per part of ethoxylated triglycerides.
8. A composition of claim 1 wherein the preservative in the oily phase is at least one ester of p-hydroxybenzoic acid in an amount of 0.2 to 4% by weight.
9. A process for the preparation of a composition of claim 1 comprising preparing an oily phase by addition of the emulsifying system, preservative and stabilizer to the oily components with stirring and heating until gelation after addition of alcohol followed by cooling to at most 30° C. and addition of the aqueous phase composed of water, preservative, glycerol, panthenol, tyrosine or tyrosine providing compound sufficient alkali and carraghenate.
10. In a method of tanning skin, the improvement comprising applying 20 to 100 ml/m2 skin area of a composition of claim 1 to the skin area involved and then subjecting the skin to the exposure of natural or artificial sunlight.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL8601767 | 1986-07-07 | ||
| NL8601767A NL8601767A (en) | 1986-07-07 | 1986-07-07 | SKIN TANNING AGENT. |
Related Parent Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/064,331 Reissue US4783332A (en) | 1986-07-07 | 1987-06-19 | Novel skin tanning composition |
| US07344203 Continuation | 1989-04-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE33845E true USRE33845E (en) | 1992-03-10 |
Family
ID=19848277
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/064,331 Ceased US4783332A (en) | 1986-07-07 | 1987-06-19 | Novel skin tanning composition |
| US07/630,822 Expired - Lifetime USRE33845E (en) | 1986-07-07 | 1990-12-20 | Novel skin tanning composition |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/064,331 Ceased US4783332A (en) | 1986-07-07 | 1987-06-19 | Novel skin tanning composition |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US4783332A (en) |
| EP (1) | EP0255964B1 (en) |
| JP (1) | JPS6322515A (en) |
| AT (1) | ATE62399T1 (en) |
| AU (1) | AU594165B2 (en) |
| CA (1) | CA1294555C (en) |
| DE (1) | DE3769240D1 (en) |
| DK (1) | DK342387A (en) |
| ES (1) | ES2021343B3 (en) |
| FI (1) | FI872962A (en) |
| GR (1) | GR3001766T3 (en) |
| NL (1) | NL8601767A (en) |
| NO (1) | NO872749L (en) |
| NZ (1) | NZ220818A (en) |
| PT (1) | PT85259B (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5484816A (en) * | 1992-07-13 | 1996-01-16 | Shiseido Company, Ltd. | External skin treatment composition |
| US6017517A (en) | 1996-12-18 | 2000-01-25 | The Dial Corporation | Method for treating human nails |
| US6036946A (en) | 1997-12-24 | 2000-03-14 | Shaklee Corporation | Methods for protecting skin from damaging effects of ultraviolet light |
| US6146664A (en) | 1998-07-10 | 2000-11-14 | Shaklee Corporation | Stable topical ascorbic acid compositions |
| US7467420B2 (en) | 2005-07-26 | 2008-12-23 | Laura Ponce | Applicator glove for application of staining compositions and self-tanning kit including same |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0203211A1 (en) * | 1985-05-28 | 1986-12-03 | Chemisch Adviesbureau Drs. J.C.P. Schreuder B.V. | Composition for treatment of skin affections and process for its preparation |
| US5290562A (en) * | 1987-11-27 | 1994-03-01 | L V M H Recherche | Compositions and methods employing liposomes including tyrosine or a tyrosine derivative |
| AU2971689A (en) * | 1988-02-11 | 1989-08-17 | Estee Lauder Inc. | Tanning compositions and their use |
| US5700450A (en) * | 1988-03-30 | 1997-12-23 | The Trustees Of Boston University | Methods for enhancing melanin synthesis in melanocytes using diacyglycerols and uses thereof |
| US5352440A (en) * | 1988-03-30 | 1994-10-04 | Trustees Of Boston University | Methods for increasing melanin content in melanocytes using diacylglycerols and uses thereof |
| DE69013020T2 (en) * | 1989-01-11 | 1995-01-26 | Schreuder Chem Adviesbureau | Aqueous skin tanning agent. |
| US20020197309A1 (en) * | 1989-09-05 | 2002-12-26 | Kuczynski Anthony L. | Method for lowering blood glucose |
| CA2053147A1 (en) * | 1990-10-15 | 1992-04-16 | Charles F. Cooper | Esterified polyoxyalkylene block copolymers as reduced calorie fat substitutes |
| US5643554A (en) * | 1993-04-30 | 1997-07-01 | Dusa Pharmaceuticals, Inc. | Lipomelanim composition |
| JPH07238010A (en) * | 1994-02-24 | 1995-09-12 | Kanebo Ltd | Skin cosmetic |
| US20030017181A1 (en) | 2001-05-31 | 2003-01-23 | Rood Gloria A. | Dermatological compositions and methods |
| US6960563B2 (en) * | 2001-08-31 | 2005-11-01 | Morton Grove Pharmaceuticals, Inc. | Spontaneous emulsions containing cyclosporine |
| DE10211752A1 (en) * | 2002-03-18 | 2003-10-02 | Richter Chem Lab | P / O emulsions containing amino functional polyols |
| US20070213409A1 (en) * | 2005-03-24 | 2007-09-13 | Beiersdorf Ag | Use of preparations for skin enzyme protection |
| US20070031357A1 (en) * | 2005-08-02 | 2007-02-08 | Anton Mentlik | High PH compositions |
| US20090246155A1 (en) * | 2006-12-05 | 2009-10-01 | Landec Corporation | Compositions and methods for personal care |
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| US3037015A (en) * | 1958-07-19 | 1962-05-29 | Benckiser Gmbh Joh A | Therapeutically valuable compounds and process of producing same |
| US3230228A (en) * | 1961-03-30 | 1966-01-18 | Hoffmann La Roche | Panthenol derivatives and processes for their preparation |
| DE2122291A1 (en) * | 1970-05-06 | 1971-11-18 | Saint-Gobain, Neuilly-sur-Seine; Etablissements Gattefosse, Saint-Priest; (Frankreich) | Sunscreen preparations and processes for their manufacture |
| FR2326914A1 (en) * | 1975-10-11 | 1977-05-06 | Lion Dentifrice Co Ltd | WATER / OIL / WATER COMPLEX EMULSION, PROCESS FOR ITS PREPARATION AND APPLICATION TO COSMETIC PRODUCTS |
| US4349536A (en) * | 1980-03-11 | 1982-09-14 | Hausler Kenneth J | Method of promoting suntan using a cream containing zinc and copper salts |
| US4690774A (en) * | 1985-09-11 | 1987-09-01 | Chesebrough Pond's Inc. | Novel translucent water in oil emulsions |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2722725A1 (en) * | 1977-05-20 | 1978-11-30 | Merck Patent Gmbh | COSMETIC MEANS |
| CA1138292A (en) * | 1978-06-30 | 1982-12-28 | Johannes C.P. Schreuder | Handwashing composition |
| CH642537A5 (en) * | 1980-01-25 | 1984-04-30 | Uni Chemie Ag | Cosmetic sunscreen product |
-
1986
- 1986-07-07 NL NL8601767A patent/NL8601767A/en not_active Application Discontinuation
-
1987
- 1987-06-12 EP EP87201116A patent/EP0255964B1/en not_active Expired - Lifetime
- 1987-06-12 AT AT87201116T patent/ATE62399T1/en not_active IP Right Cessation
- 1987-06-12 ES ES87201116T patent/ES2021343B3/en not_active Expired - Lifetime
- 1987-06-12 CA CA000539519A patent/CA1294555C/en not_active Expired - Lifetime
- 1987-06-12 DE DE8787201116T patent/DE3769240D1/en not_active Expired - Fee Related
- 1987-06-19 US US07/064,331 patent/US4783332A/en not_active Ceased
- 1987-06-23 AU AU74609/87A patent/AU594165B2/en not_active Ceased
- 1987-06-24 NZ NZ220818A patent/NZ220818A/en unknown
- 1987-07-01 NO NO872749A patent/NO872749L/en unknown
- 1987-07-03 FI FI872962A patent/FI872962A/en not_active Application Discontinuation
- 1987-07-03 DK DK342387A patent/DK342387A/en not_active Application Discontinuation
- 1987-07-03 JP JP62166762A patent/JPS6322515A/en active Pending
- 1987-07-06 PT PT85259A patent/PT85259B/en not_active IP Right Cessation
-
1990
- 1990-12-20 US US07/630,822 patent/USRE33845E/en not_active Expired - Lifetime
-
1991
- 1991-04-11 GR GR91400456T patent/GR3001766T3/en unknown
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US3037015A (en) * | 1958-07-19 | 1962-05-29 | Benckiser Gmbh Joh A | Therapeutically valuable compounds and process of producing same |
| US3230228A (en) * | 1961-03-30 | 1966-01-18 | Hoffmann La Roche | Panthenol derivatives and processes for their preparation |
| DE2122291A1 (en) * | 1970-05-06 | 1971-11-18 | Saint-Gobain, Neuilly-sur-Seine; Etablissements Gattefosse, Saint-Priest; (Frankreich) | Sunscreen preparations and processes for their manufacture |
| FR2326914A1 (en) * | 1975-10-11 | 1977-05-06 | Lion Dentifrice Co Ltd | WATER / OIL / WATER COMPLEX EMULSION, PROCESS FOR ITS PREPARATION AND APPLICATION TO COSMETIC PRODUCTS |
| US4349536A (en) * | 1980-03-11 | 1982-09-14 | Hausler Kenneth J | Method of promoting suntan using a cream containing zinc and copper salts |
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Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5484816A (en) * | 1992-07-13 | 1996-01-16 | Shiseido Company, Ltd. | External skin treatment composition |
| US6024941A (en) | 1992-07-13 | 2000-02-15 | Shiseido Company, Ltd. | External skin treatment composition |
| US6017517A (en) | 1996-12-18 | 2000-01-25 | The Dial Corporation | Method for treating human nails |
| US6036946A (en) | 1997-12-24 | 2000-03-14 | Shaklee Corporation | Methods for protecting skin from damaging effects of ultraviolet light |
| US6174519B1 (en) | 1997-12-24 | 2001-01-16 | Shaklee Corporation | Composition for protecting skin from damaging effects of ultraviolet light |
| US6146664A (en) | 1998-07-10 | 2000-11-14 | Shaklee Corporation | Stable topical ascorbic acid compositions |
| US7467420B2 (en) | 2005-07-26 | 2008-12-23 | Laura Ponce | Applicator glove for application of staining compositions and self-tanning kit including same |
| US20090100574A1 (en) * | 2005-07-26 | 2009-04-23 | Laura Ponce | Applicator Glove For Application Of Staining Compositions And Self-Tanning Kit Including Same |
Also Published As
| Publication number | Publication date |
|---|---|
| AU7460987A (en) | 1988-01-14 |
| GR3001766T3 (en) | 1992-11-23 |
| EP0255964B1 (en) | 1991-04-10 |
| EP0255964A1 (en) | 1988-02-17 |
| FI872962A (en) | 1988-01-08 |
| US4783332A (en) | 1988-11-08 |
| FI872962A0 (en) | 1987-07-03 |
| CA1294555C (en) | 1992-01-21 |
| DE3769240D1 (en) | 1991-05-16 |
| NO872749D0 (en) | 1987-07-01 |
| NZ220818A (en) | 1989-10-27 |
| AU594165B2 (en) | 1990-03-01 |
| PT85259B (en) | 1990-03-30 |
| DK342387D0 (en) | 1987-07-03 |
| NL8601767A (en) | 1988-02-01 |
| PT85259A (en) | 1987-08-01 |
| DK342387A (en) | 1988-01-08 |
| NO872749L (en) | 1988-01-08 |
| ATE62399T1 (en) | 1991-04-15 |
| JPS6322515A (en) | 1988-01-30 |
| ES2021343B3 (en) | 1991-11-01 |
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