A cosmetic composition for treating acne includes at least one acne treatment active, for example, salicylic acid or a derivative thereof, which may present in an amount that is greater than 1%, by weight, based on the weight of the sulfate-free cleansing composition, and an aqueous carrier that includes at least one surfactant selected from the group consisting of sarcosinates, betaines, and combinations thereof, at least one solubilizer comprising a polyethylene glycol compound, and water. When the sulfate-free cleansing composition is applied to a keratinous tissue it demonstrates deposition and retention of the beta hydroxy acid on the keratinous tissue after rinsing with water.

A non-rinse micellar water composition; method of manufacture for a non-rinse micellar water composition; and a method of use for a micellar water composition are disclosed.

The present invention is directed to a cosmetic composition precursor that is rapidly hydratable and conducive to creating a personalized end-product. This invention thus relates to a cosmetic composition precursor having fatty acid, inorganic base, and high HLB surfactants and methods of using said precursors in creating the end-product. The invention also relates to end-use compositions made from the hydratable cosmetic composition precursor of the invention.

In one aspect, provided is an aqueous antiseptic composition comprising glycerin 8.5-16% by weight; caprylyl glycol 0.45-3% by weight; and a first ingredient; wherein the first ingredient is acrylates/C10-30 about 0.01-0.1% by weight or ethoxydiglycol about 1-5% by weight. The glycerin, the caprylyl glycol and the first ingredient taken together form a first component. A sum of the first component is more than 13% by weight of the antiseptic composition. Other exemplary embodiments are also described. In certain embodiments, provided is an antiseptic composition useful for making skin or hand sanitizers that have a long-lasting, great antiseptic efficacy but at the same time having skin-moisturizing, low toxicity and low skin-irritating, hypo-allergenic properties, low inflammability, and low production cost.

The invention relates to a composition in the form of a nanoemulsion or microemulsion, comprising: —a first fatty acid ester of polyglycerol which is chosen from a fatty acid ester of polyglycerol formed from at least one acid comprising an alkyl or alkenyl chain containing from 12 to 20 carbon atoms and from 3 to 6 glycerol units; —a second fatty acid ester of (poly)glycerol (c) which is chosen from a fatty acid ester of (poly)glycerol formed from at least one acid comprising an alkyl or alkenyl chain containing from 6 to 18 carbon atoms and from 1 to 3 glycerol units; —at least one organopolysiloxane elastomer; —at least two acrylic acid-based polymers that are different from one another; —at least one amphiphilic polymer comprising at least one 2-acrylamidomethylpropanesulfonic acid (AMPS) unit; —at least one oil; —water. The invention also relates to a cosmetic treatment process for keratin materials such as the skin, by application of such a composition.

The invention relates to a composition in the form of a nanoemulsion or microemulsion, comprising: —a first fatty acid ester of polyglycerol which is chosen from a fatty acid ester of polyglycerol formed from at least one acid comprising an alkyl or alkenyl chain containing from 12 to 20 carbon atoms and from 3 to 6 glycerol units; —a second fatty acid ester of (poly)glycerol (c) which is chosen from a fatty acid ester of (poly)glycerol formed from at least one acid comprising an alkyl or alkenyl chain containing from 6 to 18 carbon atoms and from 1 to 3 glycerol units; —at least one organopolysiloxane elastomer; —at least two acrylic acid-based polymers that are different from one another; —at least one amphiphilic polymer comprising at least one 2-acrylamidomethylpropanesulfonic acid (AMPS) unit; —at least one oil; —water. The invention also relates to a cosmetic treatment process for keratin materials such as the skin, by application of such a composition.

The present invention relates to a water-in-oil surfactant consisting of a mixture of compounds of formula (I): ##STR00001##
wherein the compound of formula (I) has an average degree of polymerisation n of between 4 and 6,
R1, R2 and R3 being, independently of one another, a hydrogen atom or a group R4 derived from at least one carboxylic acid,
the carboxylic acid being 12-hydroxystearic acid or a mixture of 12-hydroxystearic acid and ricinoleic acid. The present invention also relates to a surfactant composition and to a cosmetic composition comprising this surfactant.

The present invention relates to a water-in-oil surfactant consisting of a mixture of compounds of formula (I): ##STR00001##
wherein the compound of formula (I) has an average degree of polymerisation n of between 4 and 6,
R1, R2 and R3 being, independently of one another, a hydrogen atom or a group R4 derived from at least one carboxylic acid,
the carboxylic acid being 12-hydroxystearic acid or a mixture of 12-hydroxystearic acid and ricinoleic acid. The present invention also relates to a surfactant composition and to a cosmetic composition comprising this surfactant.

Disclosed are stable, non-irritating, skin treatment active agents containing formulations and delivery systems for topical application to the skin. The disclosed topical formulations and delivery systems provide controlled, gentle release of the active agents into the skin for the treatment of amenable skin conditions as well as for improvement of aesthetic skin properties. Also provided are methods for the formulation, manufacture and use of the disclosed formulations and delivery systems.

A method for the synthesis of a substituted poly(alkylene oxide) comprises reacting a substituted alcohol of formula (1) with an alkylene oxide of formula (2) in the presence of a catalyst and under conditions effective to provide the substituted poly(alkylene oxide) of formula (3) wherein in the foregoing formulas, each R is independently hydrogen, C.sub.1-60 alkyl, or C.sub.3-12 cycloalkyl, ring A is cyclohexane or phenyl, each R.sup.1 is independently hydrogen, methyl, ethyl, propyl, butyl, hexyl, decyl, dodecyl, tetradecyl, or hexadecyl, preferably hydrogen or methyl, and n is 2 to 60.

##STR00001##