COMPOSITION OF CLEANSING MILK AND ITS APPLICATION

The cleansing milk composition with propylene glycol laurate, oil, and polymer improves stability and reduces greasiness, enhancing makeup removal efficacy and skin feel.

FR3168160A3Pending Publication Date: 2026-05-08LOREAL SA
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Patent Information

Authority / Receiving Office
FR · FR
Patent Type
Utility models
Current Assignee / Owner
LOREAL SA
Filing Date
2024-11-04
Publication Date
2026-05-08

AI Technical Summary

Technical Problem

Existing cleansing compositions leave a greasy feeling on the skin after makeup removal due to high oil content, affecting stability and makeup removal efficacy, leading to customer dissatisfaction.

Method used

A cleansing milk composition comprising propylene glycol laurate, at least one oil, and a polymer, with specific ratios to enhance stability and reduce greasiness while improving makeup removal.

Benefits of technology

The composition provides improved stability, enhanced makeup removal, and a less oily skin feel, addressing the imbalance between effective cleansing and skin texture.

✦ Generated by Eureka AI based on patent content.
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Abstract

CLEANSING MILK COMPOSITION AND ITS APPLICATION The present invention provides a cleansing milk composition comprising a) propylene glycol laurate; b) at least one oil; c) at least one polymer; and d) water. The composition of the present invention is a non-foaming, less greasy milky composition. The present invention also provides a method for cleaning a keratinous surface and a non-therapeutic method for removing makeup from a keratinous surface by applying the cleansing milk composition. Figure for the abstract: none
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Description

Title of the invention: Composition of cleansing milk and its application. Scope of the invention.

[0001] This disclosure relates to the field of personal care products, in particular, a cleansing milk composition. This disclosure also relates to a use of the composition for cleansing and makeup removal and associated processes. CONTEXT OF THE INVENTION

[0002] Cosmetic compositions that provide an aesthetic effect to the skin are widely used. These cosmetic products have been developed for longer wear and with transfer-resistant properties. However, removing such compositions has become a lengthy skincare routine. Therefore, a cleansing composition that can easily remove these cosmetic compositions from the keratinous surface is equally desirable.

[0003] Nevertheless, the use of such cleansing compositions presents associated challenges in achieving the desired texture, stability, and post-application effect. The use of oils in such compositions facilitates makeup removal. However, these compositions often leave a very oily or greasy feeling on the skin, which in turn necessitates the use of additional products to remove the oiliness and cleanse the skin. Thus, there has always been an imbalance between effective makeup removal and a less oily feeling after use, which has led to customer dissatisfaction with the use of these cleansers.

[0004] Therefore, there is a need to develop a cleansing composition with an optimized combination of cleansing agents, and with a desired product texture that is capable of ensuring makeup removal with less of an oily effect and cleansing the skin. Summary of the invention

[0005] In one aspect of the present invention, a cleansing milk composition is proposed comprising: a) propylene glycol laurate; b) at least one oil; c) at least one polymer; and d) water.

[0006] In another aspect of the present invention, a method for cleaning a keratinous surface is proposed, the method comprising the application of the composition as disclosed herein to the keratinous surface.

[0007] In another aspect of the present invention, a non-therapeutic makeup removal method is proposed, the method comprising the application of the composition as disclosed here on a made-up keratinous surface and rinsing to remove the makeup.

[0008] These features, aspects, and advantages, as well as others, of the present subject matter will be better understood by reference to the following description and the attached claims. This summary is provided to present a selection of concepts in a simplified form. This summary is not intended to identify key features or essential features of the claimed subject matter, nor to be used to limit the scope of the claimed subject matter. DETAILED DESCRIPTION OF THE INVENTION

[0009] Those skilled in the art will be aware that this disclosure is subject to variations and modifications other than those specifically described. It should be understood that this disclosure includes all such variations and modifications. The disclosure also includes all such steps, features, compositions, and compounds designated or indicated in this patent memorandum, individually or collectively, and any combination of one or more of these steps or features.

[0010] Definitions

[0011] For convenience, before describing this disclosure in more detail, certain terms used in the patent memorandum and examples are defined here. These definitions should be read in light of the rest of the disclosure and understood as by a person skilled in the art. The terms used here have meanings recognized and known to a person skilled in the art; however, for convenience and completeness, specific terms and their meanings are set out below.

[0012] The articles "un", "une", "la", "le" and "les" are used to designate one or more of one (i.e. at least one) grammatical object of the article.

[0013] The terms “include” and “comprising” are used in an inclusive and open sense, meaning that additional elements may be included. They are not intended to be interpreted as “consists solely of”.

[0014] The expression "at least one" is used to mean one or more and therefore includes individual components as well as mixtures / combinations.

[0015] Throughout this patent memorandum, unless the context otherwise requires, the term "include", and variations such as "includes" and "comprising", shall be understood to imply the inclusion of any element or step or group of elements or steps stated, but not the exclusion of any other element or step or group of elements or steps.

[0016] The term "including" is used to mean "including but not limited to". "Including" and "including but not limited to" are used interchangeably.

[0017] The term "approximately" is used to denote an acceptable range of error for the particular value as determined by a person skilled in the art, which may depend in part on how the value is measured or determined, i.e., on the limitations of the measuring system. For example, "approximately" may mean within 1 or more standard deviations, according to industry practice. Where particular values ​​are described in this disclosure, unless otherwise indicated, the term "approximately" shall be assumed to mean within an acceptable range of error for the particular value.

[0018] The term "INCI" is an abbreviation for International Nomenclature of Cosmetic Ingredients, which is a system of names provided by the International Nomenclature Committee of the Personal Care Products Council to identify cosmetic or personal care ingredients.

[0019] All percentages, parts, and ratios are based on the total weight of the compositions in this disclosure, unless otherwise stated. Ratios, concentrations, quantities, and other numerical data may be presented herein in a range format. It should be understood that this range format is used solely for convenience and conciseness and should be interpreted flexibly as including not only the numerical values ​​explicitly cited as the range limits, but also as including all individual numerical values ​​or subranges encompassed within that range as if each numerical value and subrange were explicitly cited.For example, a percentage range of about 0.01% to 10% should be interpreted as including not only the explicitly quoted limits of about 0.01% to about 10%, but also as including sub-ranges, such as 0.05% to 5%, 0.1% to 4%, and so on, as well as individual quantities, including fractional quantities, within the specified ranges, such as 0.10% and 0.23%, 0.45% and 0.55%, for example.

[0020] Unless otherwise defined, all technical and scientific terms used herein have the same meanings as those commonly understood by a person skilled in the art of this disclosure. Although all processes and materials similar or equivalent to those described herein may be used in the practice or testing of the disclosure, preferred processes and materials are hereby described.

[0021] This disclosure shall not be limited in scope by the specific embodiments described herein, which are intended for illustrative purposes only. Functionally equivalent products, compositions, and processes clearly fall within the scope of the disclosure as described herein.

[0022] Existing cleansing compositions contain higher quantities of oils, which affects their stability and also results in poor makeup removal capabilities. The texture of the composition and the post-application effects are also important criteria and impact customer satisfaction. Thus, a stable composition with enhanced makeup removal capabilities while leaving a less oily feeling on the skin after use was the most sought-after. Therefore, a composition with a specific combination of oils and polymers in proportional quantities was used to obtain a stable cleansing milk composition with enhanced cosmetic properties.

[0023] Accordingly, the present invention provides a cleansing milk composition comprising: a) propylene glycol laurate; b) at least one oil; c) at least one polymer; and d) water. The cleansing milk composition is a milky white composition with improved stability, the desired texture, and enhanced ease of application. The cleansing milk composition of the present invention is less foaming or non-foaming and imparts less of a greasy effect to the keratinous surface. The present invention further provides a method for cleaning a keratinous surface, the method comprising applying the composition to the keratinous surface. The present invention also provides a non-therapeutic method for removing makeup, the method comprising applying the composition to a made-up keratinous surface and rinsing to remove the makeup. Cleansing milk composition

[0024] Some embodiments of the present provide a composition, in particular a cleansing milk composition for treating and / or cleaning a keratinous surface, such as skin or lips.

[0025] Embodiments of the present formula provide a cleansing milk composition comprising a) propylene glycol laurate; b) at least one oil; c) at least one polymer; and d) water. The composition according to the present formulas comprises at least one additive selected from a pH adjuster, a preservative, a fragrance, skin actives, fillers, or combinations thereof.

[0026] The composition, according to embodiments hereof, offers both cleansing and makeup-removing properties. The composition removes makeup from a keratinous surface and is a non-foaming or low-foaming composition.

[0027] The composition, according to embodiments hereof, is a cleansing milk that acts at the interface to remove makeup and dirt molecules. The composition has a lower oil content and is a non-foaming cleansing milk. Propylene glycol laurate

[0028] Some embodiments of the present propose a cleansing milk composition comprising propylene glycol laurate.

[0029] The composition, according to embodiments hereof, includes propylene glycol laurate. Propylene glycol laurate is an amphiphile that acts at the interface between the skin and makeup and disperses makeup dirt.

[0030] According to embodiments hereof, propylene glycol laurate is present in an amount ranging from 1 to 15% by weight, preferably from 1.5 to 11% by weight, and more preferably from 1.5 to 10% by weight, relative to the total weight of the composition. Oil

[0031] Some embodiments of the present propose a cleansing milk composition comprising at least one oil.

[0032] The composition, according to embodiments of the present, comprises at least one oil.

[0033] The term "oil" refers to a fatty organic compound that is insoluble in water at 25 °C and atmospheric pressure (1.013 x 10⁵ Pa) (solubility less than 5% by weight, preferably less than 1% by weight, even more preferably less than 0.1% by weight). The oil that may be used is neither (poly)oxyalkylated nor (poly)glycerolated.

[0034] For the purposes of the present invention, the oil present in the composition is neither oxyalkylated nor glycerolated.

[0035] Preferably, the oil present in the composition of the present invention is a non-silicone oil without any Si-O bonding.

[0036] Oil is a fatty compound whose melting point is less than or equal to 25 °C at atmospheric pressure (1.013 x 0.5 Pa).

[0037] For the purposes of the present invention, the melting point corresponds to the temperature of the most endothermic peak observed in a thermal analysis (differential scanning calorimetry or DSC) as described in ISO 11357-3; 1999. The melting point can be measured using a differential scanning calorimeter (DSC), for example, the calorimeter sold under the name MDSC 2920 by TA Instruments. In this patent application, all melting points are determined at atmospheric pressure (1.013 x 1.05 Pa).

[0038] The oil, according to embodiments of the present, may be chosen from liquid hydrocarbons in the range of C6 to Ci6, liquid hydrocarbons comprising more than 16 carbon atoms, non-silicone oils of animal origin, triglyceride type oils of vegetable (vegetable oils) or synthetic origin, fluorinated oils, liquid fatty alcohols, liquid esters of fatty acids and / or fatty alcohols other than triglycerides, or combinations thereof.

[0039] Embodiments of the present formulations include a composition comprising at least one oil, preferably selected from liquid hydrocarbons in the C6 to C16 range, liquid hydrocarbons containing more than 16 carbon atoms, vegetable oils, liquid fatty alcohols, liquid fatty esters, or combinations thereof. The fatty alcohols and esters contain at least one saturated or unsaturated, linear or branched hydrocarbon-based group comprising from 6 to 40, and preferably from 8 to 30, carbon atoms, which is optionally substituted, in particular by one or more hydroxyl groups (in particular from 1 to 4). If unsaturated, these compounds may comprise one to three conjugated or non-conjugated carbon-carbon double bonds.

[0040] Liquid hydrocarbons in the C6 to Ci6 range may be linear, branched, or optionally cyclic, and are preferably chosen from among the alkanes. Examples that may be cited include hexane, cyclohexane, undecane, dodecane, isododecane, tridecane, triethylhexanoin, or isoparaffins, such as isohexadecane or isodecane, or combinations thereof.

[0041] Liquid hydrocarbons comprising more than 16 carbon atoms may be linear or branched, and of mineral or synthetic origin, and are preferably selected from liquid paraffins or liquid petroleum jelly (or mineral oil), polydecenes, hydrogenated polyisobutene such as Parleam®, and their combinations.

[0042] An oil based on hydrocarbons of animal origin that can be cited is perhydrosqualene or squalane.

[0043] The triglyceride oils of vegetable (or vegetable) or synthetic origin are preferably selected from among the triglycerides of liquid fatty acids comprising 6 to 30 carbon atoms, for example, heptanoic or octanoic acid triglycerides, or alternatively, for example, sunflower oil, corn oil, soybean oil, cucurbit oil, grapeseed oil, sesame oil, hazelnut oil, apricot oil, macadamia oil, arara oil, castor oil, avocado oil, caprylic / capric acid triglycerides, for example those sold by Stéarinerie Dubois or those sold under the names Miglyol® 810, 812 and 818 by Dynamit Nobel, jojoba oil and butter oil. Shea butter, and their combinations.

[0044] Liquid fatty alcohols suitable for use in the invention are particularly chosen from linear or branched, saturated or unsaturated alcohols, preferably unsaturated or branched alcohols, comprising from 6 to 40 carbon atoms, preferably from 8 to 30 carbon atoms. These fatty alcohols are neither oxyalkylated nor glycerolized. Examples that may be cited include octyldodecanol, 2-butyloctanol, 2-hexyldecanol, and 2-undecylpentadecanol. ol, isostearyl alcohol, oleyl alcohol, linolenylic alcohol, ricinoleyl alcohol, undecylenyl alcohol and linoleyl alcohol, or combinations thereof.

[0045] The term "fatty alcohol" refers to a long-chain aliphatic alcohol comprising from 6 to 40 carbon atoms, preferably from 8 to 30 carbon atoms, and comprising at least one hydroxyl group OH. These fatty alcohols are neither oxyalkylated nor glycerolated.

[0046] Liquid fatty esters are esters of fatty acids and / or fatty alcohols, other than the triglycerides mentioned above, including esters of saturated or unsaturated mono- or polyaliphatic acids, linear in C1 to C26 or branched in C3 to C26, and of saturated or unsaturated mono- or polyaliphatic alcohols, linear in C1 to C26 or branched in C3 to C26, the total number of carbons of the esters being greater than or equal to 6 and more advantageously greater than or equal to 10.

[0047] Preferably, for monoalcohol esters, at least one of the alcohol and the acid is branched.

[0048] Among the monoesters, the following may be mentioned: dihydroabietyl behenate, isostearyl lactate, lauryl lactate, linoleyl lactate, oleyl lactate, isostearyl octanoate, isocetyl octanoate, isocetyl isostearate, isocetyl laurate, isocetyl stearate, isodecyl octanoate, isodecyl oleate, isononyl isononanoate, isostearyl palmitate, methyl acetylricinoleate, octyl isononanoate, 2-ethylhexyl isononate, octyldodecyl erucate, oleyl erucate, palmitate ethyl, isopropyl palmitate, 2-ethylhexyl palmitate, 2-octyldecyl palmitate; alkyl myristates such as 2-octyldodecyl isopropyl myristate, isobutyl stearate; 2-hexyldecyl laurate, or combinations thereof.

[0049] Preferably, among monoesters of monoacids and monoalcohols, ethyl palmitate and isopropyl palmitate, alkyl myristates such as isopropyl myristate or ethyl myristate, isocetyl stearate, 2-ethylhexyl isononanoate, isodecyl neopentanoate and isostearyl neopentanoate, or combinations thereof, shall be used.

[0050] Esters of dicarboxylic or tricarboxylic acids in C4 to C22 and of alcohols in C1 to C22 and esters of monocarboxylic, dicarboxylic or tricarboxylic acids and of dihydroxy, trihydroxy, tetrahydroxy or pentahydroxy alcohols in C2 to C26 may also be used.

[0051] Examples include diethyl sebacate, diisopropyl sebacate, diisopropyl adipate, di-n-propyl adipate, dioctyl adipate, diisostearyl adipate, dioctyl maleate, glyceryl undecylenate, octyldodecyl stearoyl stearate, pentraerythrityl monoricinoleate, and tetraisononanoate. pentaerythrityl, pentaerythrityl tetrapelargonate, pentaerythrityl tetraisostearate, pentaerythrityl tetraoctanoate, propylene glycol dicaprylate, propylene glycol dicaprate, tridecyl erucate, triisopropyl citrate, triisostearyl citrate; glyceryl trilactate, trioctyldodecyl citrate, trioleyl citrate, propylene glycol dioctanoate, neopentyl glycol diheptanoate, diethylene glycol diisononanoate, polyethylene glycol distearates, or combinations thereof.

[0052] The composition may also include, as a fatty acid ester, sugar esters and diesters of fatty acids in the C6 to C30 range and preferably in the C2 to C22 range. The term "sugar" refers to compounds based on oxygen-bearing hydrocarbons bearing several alcohol functional groups, with or without aldehyde or ketone functional groups, and comprising at least four carbon atoms. These sugars may be monosaccharides, oligosaccharides, or polysaccharides.

[0053] Examples of suitable sugars that may be cited include sucrose, glucose, galactose, ribose, fucose, maltose, fructose, mannose, arabinose, xylose, and lactose and their derivatives, including alkyl derivatives, such as methyl derivatives, for example methylglucose.

[0054] Sugar esters of fatty acids may be selected in particular from the group comprising the esters or mixtures of esters of sugars described above and of linear or branched fatty acids, saturated or unsaturated in C6 to C30 and preferably in Ci2 to C22. If they are unsaturated, these compounds may comprise one to three conjugated or non-conjugated carbon-carbon double bonds.

[0055] Esters can also be chosen from monoesters, diesters, triesters, tetraesters, polyesters, or combinations thereof.

[0056] These esters may be, for example, oleates, laurates, palmitates, myristates, behenates, cocoates, stearates, linoleates, linolenates, caprates, arachidonates, or combinations thereof, in particular such as mixed esters of oleopalmitate, oleostearate and palmitostearate.

[0057] More specifically, monoesters and diesters are used, and in particular mono- or dioleates, stearates, behenates, oleopalmitates, linoleates, linolenates and oleostearates of sucrose, glucose or methylglucose, or combinations thereof. An example that can be cited is the product sold under the name Glucate® DO by the company Amerchol, which is a methylglucose dioleate.

[0058] Preferably, a liquid ester of a monoacid and a monoalcohol will be used.

[0059] The oil, according to embodiments of the present, is preferably chosen from liquid hydrocarbons containing more than 16 carbon atoms, vegetable oils, liquid fatty alcohols and liquid fatty esters, or combinations thereof.

[0060] According to embodiments of the present, the oil is in an amount ranging from 1% to 12% by weight, and preferably from 2% to 12% by weight, relative to the total weight of the composition. Polymer

[0061] Some embodiments of the present propose a cleansing milk composition comprising at least one polymer.

[0062] For the purposes of the invention, the term "polymer" means any compound derived from the polycondensation polymerization or radical polymerization of monomers, at least one of which is other than an alkylene oxide, and a monofunctional compound of formula RX, R designating an optionally hydroxylated Ci0-C30 alkyl or alkenyl group, and X designating a hydroxylated carboxylic acid, amine, amide or ester group.

[0063] The cleansing milk composition, according to embodiments of the present, comprises at least one polymer selected from associative polymers, non-associative polymers, or combinations thereof.

[0064] The composition, according to embodiments of the present, comprises at least one polymer selected from an anionic associative polymer, a non-ionic associative polymer, a non-associative polymer, or combinations thereof.

[0065] According to embodiments of the present, the polymer is in an amount ranging from 0.01 to 10% by weight, preferably from 0.1 to 5% by weight, and more preferably from 0.1 to 1% by weight, relative to the total weight of the composition.

[0066] Associative Polymers

[0067] The composition according to embodiments of the present may include at least one associative polymer such as an anionic associative polymer, a non-ionic associative polymer, or combinations thereof.

[0068] For the purposes of the present invention, the term "associative polymer" refers to an amphiphilic polymer that is capable, in an aqueous medium, of reversibly associating with itself or with other molecules. It generally includes, in its chemical structure, at least one hydrophilic region or group and at least one hydrophobic region or group.

[0069] Associative polymers are polymers comprising at least one fatty chain including 8 to 30 carbon atoms, whose molecules are capable, in the formulation medium, of associating with each other or with molecules of other compounds. Preferably, the fatty chain includes 10 to 30 carbon atoms.

[0070] Anionic associative polymers

[0071] The composition according to embodiments of the present may include at least one anionic associative polymer.

[0072] Among anionic associative polymers, the following may be mentioned in particular: A. those including at least one hydrophilic motif and at least one fatty-chain allylic ether motif; and more particularly, those:

[0073] whose hydrophilic motif consists of an unsaturated ethylenic anionic monomer, more particularly of a vinylcarboxylic acid and especially of an acrylic acid or a methacrylic acid, or combinations thereof; and

[0074] whose fatty-chain allyl ether motif corresponds to the monomer of formula (!') below: CH2=C(R')-CH2OBnR

[0075] in which R' denotes H or CH3, B denotes an ethyleneoxy radical, n ranges from 0 to 100 and R denotes a hydrocarbon-based radical selected from alkyl, arylalkyl, aryl, alkylaryl and cycloalkyl radicals, comprising from 8 to 30 carbon atoms, preferably from 10 to 24 carbon atoms and even more particularly from 12 to 18 carbon atoms. Preferably, R' denotes H, n = 10 and R denotes a stearyl radical (Ci8).

[0076] Among these anionic associative polymers, polymers formed from 20% to 60% by weight of acrylic acid and / or methacrylic acid, from 5% to 60% by weight of C1-C4 alkyl (meth)acrylates, from 2% to 50% by weight of fatty chain allyl ether and from 0% to 1% by weight of a crosslinking agent which is preferably a copolymerizable unsaturated polyethylene monomer, such as diallyl phthalate, allyl (meth)acrylate, divinylbenzene, (poly)ethylene glycol dimethacrylate or methylenebisacrylamide.

[0077] Preference is more particularly given to crosslinked terpolymers of methacrylic acid, ethyl acrylate and polyethylene glycol (10 EO) stearyl alcohol ether (Steareth-10), in particular the product sold by BASF under the name Salcare SC80, which is a 30% aqueous emulsion of a crosslinked terpolymer of methacrylic acid, ethyl acrylate and Steareth-10 allylic ether (40 / 50 / 10) having the INCI name Steareth-10 Allyl Ether / Acrylates Copolymer; A. those including at least one hydrophilic motif of the unsaturated olefinic carboxylic acid type, and at least one hydrophobic motif of the unsaturated carboxylic acid (C10-C30) alkyl ester type.

[0078] These polymers are preferably chosen from those in which the hydrophilic motif of the unsaturated olefinic carboxylic acid type corresponds to the monomer of formula (II) below: — C—OH p|) R: O

[0079] in which Ri denotes H or CH3 or C2H5, and in which the hydrophobic alkyl ester (Ci0-C30) motif of the unsaturated carboxylic acid type corresponds to the monomer of formula (III) below: CH ---------- CC ■■■■■■■■■■■' OR 11 ) p, O

[0080] in which R2 designates H, CH3 or C2H5 and R3 designates an alkyl radical in Ci0-C30 and preferably in Ci2-C22.

[0081] Alkyl esters in C10-C30 of unsaturated carboxylic acids according to the present invention include, for example, lauryl acrylate, stearyl acrylate, decyl acrylate, isodecyl acrylate and dodecyl acrylate, and the corresponding methacrylates, lauryl methacrylate, stearyl methacrylate, decyl methacrylate, isodecyl methacrylate and dodecyl methacrylate.

[0082] Among these anionic associative polymers, polymers formed from a mixture of monomers comprising will be used in particular: i. (meth)acrylic acid, ii. an ester of formula (III) described above in which R2 denotes H or CH3, R3 denotes an alkyl radical having from 12 to 22 carbon atoms, and optionally iii. and a crosslinking agent which is a well-known copolymerizable unsaturated polyethylene monomer, for example diallyl phthalate, allyl (meth)acrylate, divinylbenzene, (poly)ethylene glycol dimethacrylate or methyl lenebis acrylamide.

[0083] Among anionic associative polymers of this type, preference is given more particularly to those consisting of 95% to 60% by weight of (meth)acrylic acid, 4% to 40% by weight of alkyl acrylate in Ci0-C30 and 0% to 6% by weight of polymerizable crosslinking monomer, or to those consisting of 98% to 96% by weight of (meth)acrylic acid, 1% to 4% by weight of alkyl acrylate in Ci0-C30 and 0.1% to 0.6% by weight of polymerizable crosslinking monomer, such as those described above.

[0084] Examples include products sold by Lubrizol under the trade names Pemulen TRI, Pemulen TR2, Carbopol 1382, Carbopol ETD 2020, Carbopol Ultrez 20, and Carbopol Ultrez 21, with the INCI name Acrylates / C10-30 Alkyl Acrylate Crosspolymer, and even more preferably Pemulen TRI and Carbopol 1382; A. Maleic anhydride / α-olefin C30-C38 / alkyl maleate terpolymers, such as maleic anhydride / α-olefin C30-C38 / isopropyl maleate copolymer, in particular the product sold under the name Performa V 1608 by Newphase Technologies (INCI name: C30-38 Olefin / Isopropyl Maleate / MA Copolymer); B. acrylic terpolymers comprising (a) 20% to 70% by weight of an α,[3-monoethylenically unsaturated carboxylic acid, (b) 20% to 80% by weight of a non-surfactant α,[3-monoethylenically unsaturated monomer other than (a), and (c) 0.5% to 60% by weight of a nonionic monourethane which is the reaction product of a monohydric surfactant with a monoethylenically unsaturated monoisocyanate.

[0085] In particular, one can cite methacrylic acid / methyl acrylate / dimethyl(meta-isopropenyl)benzyl terpolymer of ethoxylated behenyl alcohol (40 EO), especially in the form of a 25% aqueous dispersion, such as the Viscophobe DB1000 product sold by the company Amerchol (Dow Chemical), under the INCI name Polyacrylate-3. A. copolymers of monomers (i) an α,[3-monoethylenically unsaturated carboxylic acid, such as acrylic or methacrylic acid, and (ii) an ester of an α,[3-monoethylenically unsaturated carboxylic acid, in particular acrylic or methacrylic acid, and fatty alcohol, in particular C8-C32> fatty alcohol which is oxyalkylened, comprising in particular 2 to 100 mol of ethylene oxide, in particular 4 to 50, or even 10 to 40 EO.

[0086] Examples of monomers include behenyl or stearyl (meth)acrylate comprising 10 to 40 EO, in particular 18 to 30 EO.

[0087] Preferably, these compounds also comprise as a monomer an ester of an α,[3-monoethylenically unsaturated carboxylic acid and a Ci-C4 alcohol, in particular a Ci-C4 alkyl (meth)acrylate. Preferably, these copolymers comprise at least one (meth)acrylic acid monomer, at least one CrC4 alkyl (meth)acrylate monomer and at least one C8-C32 alkyl (meth)acrylate monomer which is oxyethylenated, comprising from 2 to 100 mol EO, in particular from 4 to 50 EO, or even from 10 to 40 EO.

[0088] By way of example, one can cite Aculyn 22 sold by Rohm and Haas, which is an oxyalkylated methacrylic acid / ethyl acrylate / stearyl methacrylate terpolymer (INCI name: Acrylates / Steareth-20 Methacrylate Copolymer), or also Aculyn 28 sold by Rohm and Haas, which is a methacrylic acid terpolymer oxyalkylened / ethyl acrylate / behenyl methacrylate (INCI name: Acrylates / Beheneth-25 Methacrylate Copolymer) and also the Novethix L-10 polymer sold by Lubrizol. A. associative polymers including at least one ethylenically unsaturated monomer bearing a sulfonic group, in free form or partially or totally neutralized and comprising at least one hydrophobic part.

[0089] Among polymers of this type, special mention may be made of crosslinked or non-crosslinked, neutralized or non-neutralized copolymers including 15% to 60% by weight of AMPS (2-acrylamido-2-methylpropanesulfonic acid or salt) motifs and 40% to 85% by weight of alkyl (C8-Ci6) (meth)acrylate motifs relative to the polymer, such as those described in patent application EP-A-750 899; - terpolymers including 10% to 90% mol of acrylamide motifs, 0.1% to 10% mol of AMPS motifs and 5% to 80% mol of n-(C6-C8)alkylacrylamide motifs, such as those described in US patent 5 089 578; copolymers of totally neutralized AMPS and dodecyl methacrylate, and also copolymers of AMPS and n-dodecylmethacrylamide, which are non-crosslinked and crosslinked;copolymers consisting of AMPS motifs and steareth-25 methacrylate motifs, such as Aristoflex HMS® sold by Clariant (INCI name: Ammonium Acryloyldimethyltaurate / Steareth-25 Methacrylate Crosspolymer), or of beheneth-25 methacrylate motifs, such as Aristoflex HMB (INCI name: Ammonium Acryloyldimethyltaurate / Beheneth-25 Methacrylate Crosspolymer) sold by Clariant, or also of steareth-8 methacrylate motifs, such as Aristoflex SNC® from Clariant (INCI name: Ammonium Acryloyldimethyltaurate / Steareth-8 Methacrylate Copolymer). A. associative polymers including at least one vinyllactam monomer and at least one α,[3-monoethylenically unsaturated carboxylic acid monomer, such as vinylpyrrolidone, acrylic acid and Ci-C20 alkyl methacrylate terpolymers, for example lauryl methacrylate, such as the product sold by ISP under the name Acrylidone® LM (INCI name: VP / Acrylates / Lauryl Methacrylate Copolymer).

[0090] The anionic associative polymer, according to embodiments of the present, is preferably selected from copolymers of monomers of (i) an α,[3-monoethylenically unsaturated carboxylic acid, such as acrylic or methacrylic acid, and (ii) an ester of an α,[3-monoethylenically unsaturated carboxylic acid, in particular acrylic or methacrylic acid, and fatty alcohol, in particular a C8-C32j fatty alcohol which is oxyalkylened, comprising in particular 2 to 100 mol of ethylene oxide, in particular 4 to 50, or even 10 to 40 EO.

[0091] According to embodiments of the present, the anionic associative polymer is in an amount ranging from 0.01 to 10% by weight, preferably from 0.1 to 5% by weight, and more preferably from 0.1 to 1% by weight, relative to the total weight of the composition.

[0092] Non-ionic associative polymers

[0093] The composition, according to embodiments of the present, may comprise at least one non-ionic associative polymer.

[0094] Non-ionic associative polymers are preferably selected, alone or in mixtures, from: 1. Cellulose or modified cellulose; cellulose may be modified with groups including at least one fatty chain, in particular an alkyl group at C8-C32 and preferably at C14-C28; preferably from:

[0095] - hydroxyethylcelluloses, hydroxypropylcelluloses or hydroxyethylcelluloses, modified hydroxypropylcelluloses with groups including at least one fatty chain, in particular alkyl in the C8-C32 and, better still, in the C14-C28, such as alkyl, arylalkyl or alkylaryl groups, or combinations thereof, and in which the alkyl groups are preferably in the C8-C22, for example cetylhydroxyethylcellulose sold in particular under the reference Natrosol Plus Grade 330 CS (C16 alkyls) sold by the Ashland company, or the product Polysurf 67CS sold by the Ashland company,

[0096] - hydroxyethylcelluloses modified by alkylphenol ether groups of polyalkylene glycol, such as the Amercell Polymer HM-1500 product (nonylphenyl polyethylene glycol ether (15)) sold by the Amerchol company,

[0097] - or combinations thereof. 1. Hydroxypropyl guars modified by groups including at least one fatty chain, in particular alkyl in C8-C32 and better still, in C[4-C28, such as the product Esaflor HM 22 (alkyl chain in C22) sold by the company Lamberti, and the products RE210-18 (alkyl chain in Ci4) and RE205-1 (alkyl chain in C20) sold by the company Rhodia. 2. Copolymers of vinylpyrrolidone and hydrophobic fat-chain monomers, particularly alkyl monomers in the C8-C32 and, even better, in the C14-C28 range. Examples that can be cited include:

[0098] - the vinylpyrrolidone / hexadecene copolymer and, in particular, the products Antaron V216 or Ganex V216 sold by the company ISP;

[0099] - vinylpyrrolidone / eicosene copolymer and, in particular, Antaron products V220 or Ganex V220 sold by the company ISP. 1. Copolymers of C1-C6 methylacrylates or alkyl acrylates and amphiphilic monomers including at least one fatty chain, in particular an alkyl chain in C8-C32 and even better, in CM-C28, for example the methyl acrylate / oxyethylenated stearyl acrylate copolymer sold by the Goldschmidt Company under the name Antil 208. 2. Copolymers of methacrylates or hydrophilic acrylates and hydrophobic monomers including at least one fatty chain, in particular an alkyl chain in C8-C32 and better still, in Ci4-C28, for example polyethylene glycol methacrylate / lauryl methacrylate copolymer. 3. Polyurethane polyethers including in their chain both hydrophilic blocks usually of polyoxyethylenated nature and hydrophobic blocks, which may be aliphatic sequences alone and / or cycloaliphatic and / or aromatic sequences. 4. Polymers comprising an aminoplast ether skeleton having at least one fatty chain, in particular alkyl in C8-C32 and better still, in C[4-C28, such as the Pure Thix compounds sold by the Süd-Chemie company.

[0100] Preferably, the polyether polyurethanes comprise at least two lipophilic hydrocarbon-based chains having from 8 to 30 carbon atoms, separated by a hydrophilic block, wherein the hydrocarbon-based chains may be dangling chains or chains at the end of the hydrophilic block. In particular, one or more dangling chains may be envisaged. Furthermore, the polymer may include a hydrocarbon-based chain at one or both ends of a hydrophilic block.

[0101] Polyurethane polyethers can be multiblock, particularly in triblock form. The hydrophobic blocks can be at each end of the chain (e.g., a triblock copolymer with a central hydrophilic block) or distributed both at the ends and in the chain (e.g., a multiblock copolymer). These same polymers can also be grafted polymers or star polymers.

[0102] Nonionic fat-chain polyether polyurethanes can be triblock copolymers whose hydrophilic sequence is a polyoxyethylenated chain including 50 to 1000 oxyethylenated groups. Nonionic polyurethane polyethers comprise a urethane bond between the hydrophilic blocks, hence their name.

[0103] By extension, non-ionic fat-chain polyether polyurethanes are also included among those in which the hydrophilic blocks are linked to the lipophilic blocks via other chemical bonds.

[0104] By way of examples of nonionic fatty-chain polyether polyurethanes that can be used in the invention, Rheolate 205® containing a urea function, sold by Rheox, or Rheolate® 208, 204 or 212, as well as Acrysol RM 184®, can also be used. Elfacos T210® can also be mentioned. containing a C12-C14 alkyl chain, and the Elfacos T212® product containing a Ci8 alkyl chain, from Akzo. Alternatively, the DW 1206B® product from Rohm & Haas, containing a C2O alkyl chain and a urethane bond, supplied at a solids content of 20% in water, can be used.

[0105] Solutions or dispersions of these polymers can also be used, particularly in water or in aqueous / alcoholic media. Examples of such polymers include Rheolate® 255, Rheolate® 278, and Rheolate® 244, sold by Rheox. Products DW 1206F and DW 1206J, sold by Rohm & Haas, can also be used.

[0106] Polyurethane polyethers which can be used according to the invention are in particular those described in the article by G. Fonnum, J. Bakke and Fk. Hansen - Colloid Polym. Sci. 271, 380.389 (1993).

[0107] Even more particularly, it is preferable to use a polyether polyurethane which can be obtained by polycondensation of at least three compounds comprising i. at least one polyethylene glycol comprising 150 to 180 mol of ethylene oxide, ii. stearyl alcohol or decyl alcohol, and iii. at least one diisocyanate.

[0108] These polyether polyurethanes are sold in particular by the company Rohm & Haas under the names Aculyn 46® and Aculyn 44® [Aculyn 46® is a polyethylene glycol polycondensate having 150 or 180 mol of ethylene oxide, stearyl alcohol and methylenebis(4-cyclohexyl isocyanate) (SMDI), at 15% by weight in a matrix of maltodextrin (4%) and water (81%); Aculyn 44® is a polyethylene glycol polycondensate having 150 or 180 mol of ethylene oxide, decyl alcohol and methylenebis(4-cyclohexyl isocyanate) (SMDI), at 35% by weight in a mixture of propylene glycol (39%) and water (26%)].

[0109] The non-ionic associative polymer, according to embodiments of the present, is chosen from celluloses or modified celluloses, preferably chosen from hydroxyethylcelluloses, modified hydroxypropylmethylcelluloses, modified hydroxypropylmethylcelluloses, or combinations thereof.

[0110] According to embodiments of the present, the non-ionic associative polymer is in an amount ranging from 0.01 to 10% by weight, preferably from 0.1 to 5% by weight, and more preferably from 0.1 to 1% by weight, relative to the total weight of the composition. [YES] Non-associative polymer

[0112] The composition, according to embodiments of the present, may comprise at least one non-associative polymer.

[0113] The non-associative anionic acrylic polymer contains hydrophilic motifs of unsaturated olefinic carboxylic acid, and potentially in the presence of at least one crosslinking agent.

[0114] The non-associative anionic acrylic polymer may be selected from those obtained from at least one monomer of formula (I) below: / R'c (II) R'— C=C a H \ O (3)

[0115] wherein R'a represents a hydrogen atom, or a linear or branched alkyl group (in C1-C6), preferably R'a represents a hydrogen atom, a methyl group, or an ethyl group, more preferably a hydrogen atom; R'c represents a hydrogen atom, a linear or branched alkyl group (in C1-C6), a C(O)OX group, or an -alk-C(O)OX group, wherein X represents a hydrogen atom, an alkali metal, an alkaline earth metal, or an ammonium and -alk- represents an alkylene group (in C1-C6) such as the methylene group, preferably R'c represents a hydrogen atom, a methyl group, an ethyl group, a C(O)OH group; more preferably a hydrogen group; and Ri represents a hydrogen atom, an alkali metal, an alkali metal, or an alkyl group (in Ci-C6), preferably a hydrogen atom;More specifically, R'a represents a hydrogen atom, R'c represents a hydrogen atom, a methyl group or an ethyl group provided that at least one monomer is such that Ri represents a hydrogen atom, an alkali metal or an alkaline earth metal.

[0116] According to a particular embodiment, the polymer is obtained from a monomer of formula (I) as defined above with Ri representing a hydrogen atom, an alkali metal or an alkaline earth metal.

[0117] According to another embodiment, the non-associative anionic acrylic polymer is a homopolymer obtained from acrylic acid monomers or methacrylic acid monomers, preferably from acrylic acid monomers. The non-associative anionic acrylic polymer may be crosslinked by a crosslinking agent.

[0118] The expression "crosslinking agent" refers to an agent capable of creating links between molecular chains to form a three-dimensional network of linked molecules of (co) or (homo)polymers.

[0119] More specifically, the crosslinking agent is chosen from a monomer containing at least one ethylenyl or allyether group such as the following formula (IV) or (V):

[0120] wherein R"c represents a hydrogen atom, a linear or branched alkyl group (in Ci-C6), a C(O)OX group, or an -alk-C(O)OX group, wherein X represents a hydrogen atom, an alkali metal, an alkaline earth metal, or an ammonium, and -alk- represents an alkylene group (in Ci-C6) such as the methylene group, more particularly represents H or a methyl group, and at least one other polymerizable group whose unsaturated bonds are not conjugated to each other.

[0121] Examples include ethylene glycol di(meth)acrylate derivatives such as ethylene glycol diacrylate, di(ethylene glycol) diacrylate, tetra(ethylene glycol) diacrylate, ethylene glycol dimethacrylate, di(ethylene glycol) dimethacrylate, tri(ethylene glycol) dimethacrylate; methylenebisacrylamide derivatives such as N,N-methylenebisacrylamide, N,N-methylenebisacrylamide, N,N-(1,2-dihydroxyethylene)bisacrylamide; a formaldehyde-free crosslinking agent such as N-(l-hydroxy-2,2-dimethoxyethyl)acrylamide and divinylbenzene; and a (poly)allylether such as (poly)allylsucrose, (poly)allylpentaerythritol, or a combination thereof, preferably (poly)allylethers such as (poly)allylsucrose, (poly)allylpentaerythritol, or one of their combinations.

[0122] Preferably, the monomers of formula (I) are polymerized in the presence of a crosslinking agent, in particular in the presence of (poly)allylethers, especially (poly)allylsucrose and (poly)allylpentaerythritol such as carbomers which correspond to a homopolymer of acrylic acid crosslinked with a pentaerythritol allylether, a sucrose allylether, or a propylene allylether.

[0123] These carbomers are sold, for example, under the trade name Carbopol® 940, Carbopol® 941, Carbopol® 980, Carbopol® 981. More preferably, Carbopol® 980, Carbopol® 981, or combinations thereof.

[0124] In some embodiments, the non-associative anionic acrylic polymer is selected from an acrylic acid homopolymer crosslinked with a pentaerythritol allylether, a sucrose allylether or a propylene allylether.

[0125] According to embodiments hereof, the non-associative polymer is present in an amount ranging from 0.01 to 10% by weight, preferably from 0.1 to 5% by weight, and more preferably from 0.1 to 1% by weight, relative to the total weight of the composition. Polyol

[0126] Some embodiments of the present propose a cleansing milk composition comprising at least one polyol.

[0127] For the purposes of the present invention, the term "polyol" means an organic compound consisting of a hydrocarbon-based chain optionally interrupted by one or more oxygen atoms and bearing at least two free hydroxyl groups (-OH) on different carbon atoms, this compound being optionally cyclic or acyclic, linear or branched, and saturated or unsaturated.

[0128] The polyol, according to embodiments of the present, comprises 2 to 30 hydroxyl groups, preferably 2 to 10 hydroxyl groups, and more preferably 2 to 3 hydroxyl groups.

[0129] In some embodiments, the polyol(s) that may be used is / are selected from diglycerol, glycerol, propylene glycol, propanediol, 1,3-butylene glycol, pentane-1,2-diol, octane-1,2-diol, dipropylene glycol, hexylene glycol, ethylene glycol, polyethylene glycols, caprylyl glycol, sorbitol, sugars such as glucose, or combinations thereof, preferably from glycerol, propane-1,3-diol, caprylyl glycol, or combinations thereof. In some embodiments, the polyol is selected from propane-1,3-diol, glycerol, or combinations thereof.

[0130] According to embodiments hereof, the polyol(s) is / are in an amount ranging from 0.01% to 15% by weight, preferably from 0.1% to 10% by weight, and more preferably from 0.2% to 8% by weight, relative to the total weight of the composition. Water

[0131] Some embodiments of the present propose a cleansing milk composition comprising water.

[0132] According to embodiments of the present, the water is in a quantity ranging from 10% to 90% by weight, and preferably from 20% to 80% by weight, relative to the total weight of the composition. Additives

[0133] The composition of cleansing milk, according to embodiments of the present, may include at least one additive, chosen from a pH correcting agent, a preservative, a perfume, skin actives, fillers, or combinations thereof.

[0134] The composition of cleansing milk, according to embodiments hereof, includes at least one pH correcting agent.

[0135] In some embodiments, the pH correcting agent that can be used is chosen from aqueous ammonia, alkali metal carbonates or bicarbonates such as sodium (hydrogen)carbonate and potassium (hydrogen)carbonate, alkali metal or alkaline earth metal phosphates such as sodium phosphates or potassium phosphates, sodium or potassium hydroxides, alkali metal or alkaline earth metal silicates or metasilicates such as sodium metasilicate, citrates, phosphates, or combinations thereof.

[0136] In some embodiments, the pH correcting agent that can be used is chosen from alkanolamines, amino acids, organic amines other than alkanolamines, oxyethylenated and / or oxypropylenated ethylenediamines, 1,3-diaminopropane, spermine, spermidine, or combinations thereof.

[0137] The cleansing milk composition, according to embodiments herein, includes at least one preservative, which is used to protect the composition from microbial contamination and / or any associated degradation of the composition.

[0138] Examples of preservatives include, but are not limited to, parabens, methylisothiazolinone, benzisothiazolinone, methylchloroisothiazolinone, benzyl alcohol, salicylic acid, sorbic acid, sodium benzoate, potassium sorbate, or combinations thereof.

[0139] The cleansing milk composition, according to embodiments herein, includes at least one fragrance, which is used to impart a pleasant aroma to the composition and to mask any undesirable odor that may arise from the other ingredients of the composition. Furthermore, the fragrances provide a pleasant sensory experience to the user during the use of the composition.

[0140] In some embodiments, the fragrance is a mixture of essential oils.

[0141] The composition of the cleansing milk, according to embodiments herein, may also include at least one skin active ingredient selected from a cooling agent, an antioxidant, a skin-conditioning agent, an exfoliating agent, antioxidants, anti-inflammatory compounds, and antimicrobials, or combinations thereof. The active ingredient is selected so as to confer the enhanced cosmetic effect such as cooling, anti-exfoliating, antimicrobial, gentle exfoliating, antioxidant, skin-conditioning, skin-repairing, sebum-regulating, anti-acne, etc.

[0142] The cleansing milk composition, according to embodiments hereof, comprises a skin active ingredient selected from menthol, methyl diisopropyl propionamide, menthyl lactate, menthone glycerin acetal, menthyl lactate, ethyl menthane carboxamide, menthoxypropanediol, vitamin E, salicylic acid, beta hydroxybutanoic acid, tropic acid, trethocanic acid, panthenol, lactic acid, glycolic acid, mandelic acid, citric acid, malic acid, tartaric acid, lactobionic acid, gluconic acid or an ester thereof. ci, zinc gluconate, zinc sulfate, zinc salt of pyrrolidone carboxylic acid, vitamin B2, vitamin B6, vitamin C, ascorbyl glucoside, ascorbyl tetraisopalmitate, ascorbyl magnesium phosphate, phenoxyethanol, niacinamide, or combinations thereof.

[0143] The cleansing milk composition, according to embodiments of the present, may also include at least one filler selected from starch, TiO2, rice powder, clay, talc, silica, acrylic copolymer powders; polyethylene powders; polyamide powders, or combinations thereof.

[0144] In some embodiments, charges stimulate the sebum control components in the skin.

[0145] It is understood that a person skilled in the art will take care to select the optional additives and / or their quantity so that the advantageous properties of the composition used according to the invention are not, or not substantially, adversely affected by the envisaged addition. All these embodiments, including the optional additives, are understood to be included within the scope of the present invention. Product

[0146] Some embodiments of the present provide a product comprising a cleansing milk composition.

[0147] The product, according to embodiments herein, is in particular a cleansing milk composition for cleaning keratinous surfaces, such as skin or lips. Preferably, the composition, according to embodiments herein, is a composition for cleansing and removing makeup. More preferably, the composition provides instant makeup removal with less oiliness. The product, according to embodiments herein, may be in the form of a milk, a lotion, or a gel.

[0148] The product, according to embodiments herein, is a milky white composition, less foaming or non-foaming. The composition, according to embodiments herein, can be applied to the keratinous surface, followed by working the composition and wiping or rinsing the composition. It is possible to leave the composition according to the present invention on the keratinous surface for a certain period, such as a few minutes, after its application to the keratinous surface and before wiping / rinsing to enhance the desired cosmetic benefits. The composition, according to embodiments herein, can be used to remove makeup from a keratinous surface. Method and use

[0149] Some embodiments of the present provide a method for cleaning a keratinous surface such as skin or lips.

[0150] The process, according to embodiments of the present, comprises applying the composition of the present invention to the keratinous surface.

[0151] Some embodiments of the present invention propose a non-therapeutic makeup removal method. According to some embodiments of the present invention, the method comprises applying the composition of the present invention 1 to a keratinized surface covered with makeup and rinsing or wiping to remove the makeup.

[0152] The process of the present invention removes makeup from the keratinous surface. The process of the present invention is less foaming or non-foaming.

[0153] Embodiments of the present propose a use of the cleansing milk composition according to the present invention.

[0154] The cleansing milk composition, according to embodiments herein, can be used to cleanse and remove makeup from a keratinous surface, in particular the skin or lips. Furthermore, the composition leaves a less greasy effect on the keratinous surface.

[0155] The cleansing milk composition, according to embodiments of the present, can be applied to the keratinous surface, followed by working the composition according to a non-foaming or low-foaming behavior and wiping or rinsing the composition.

[0156] It is possible to leave the composition according to this disclosure on the keratinous surface for a certain period, such as a few minutes, after its application to the keratinous surface and before wiping / rinsing to enhance the makeup removal capacity and the desired skin cleansing benefits.

[0157] Although the subject has been described in great detail with reference to certain examples and implementations thereof, it is understood that other implementations are possible and included within the scope of the present invention. EXAMPLES

[0158] The disclosure will now be illustrated by practical examples, which are intended to demonstrate how the disclosure works and are not intended to be restrictive in any way that would limit the scope of this disclosure. Unless otherwise defined, all technical and scientific terms and expressions used herein have the same meanings as those commonly understood by a person skilled in the art of this disclosure. Although processes and materials similar or equivalent to those described herein may be used in practice for the disclosed processes and compositions, examples of such processes, devices, and materials are described herein. It should be understood that this disclosure is not limited to the particular processes and experimental conditions described, as such processes and conditions may be applicable.

[0159] In the following examples, unless otherwise indicated, percentages are given as a percentage of the total weight of the composition. The percentages are percentages by weight per active ingredient or active substance. Example 1

[0160] Composition Cl (according to the present invention) was prepared by mixing the components in a specified weight and a sufficient quantity of water as shown in Table 1. Similarly, compositions C2, C3, C4 and C5 were also prepared by varying the amount of propylene glycol laurate as mentioned in Table 1 below.

[0161] The comparative CPI composition was prepared by mixing said components as mentioned in Table 1 without propylene glycol laurate.

[0162] [Tables 1] Ingredients (INCI) % by weight Cl C2 C3 C4 C5 CPI Propylene Glycol Laurate 1.5 5.0 10.0 3.0 3.0 - Salicylic Acid 0.20 0.20 0.20 0.20 0.20 0.20 Sodium Hydroxide 0.13 0.13 0.13 0.13 0.13 0.13 Glycerin 3.00 3.00 3.00 3.00 3.00 3.00 Propanediol 3.00 3.00 3.00 3.00 3.00 3.00 Caprylyl Glycol 0.30 0.30 0.30 0.30 0.30 0.30 Isopropyl palmitate 11.50 8.00 3.00 - - 13.00 Triethylhexanoin - - - 10.00 - - Squalane - - - - 10.00 - Carbomer 0.40 0.40 0.40 0.40 0.40 0.40 Acrylates / Cio-3O alkyl acrylate crosspolymer 0.15 0.15 0.15 0.15 0.15 0.15 Water (Water) Qs 100 Qs 100 Qs 100 Qs 100 Qs 100 Qs 100 Example 2 Makeup removal capacity

[0163] For the purposes of this disclosure for the makeup removal studies, a frictiometer (Tribomaster TL-201- Sa Trinity Lab, Inc) and a colorimeter (Spectrophorometer Konica Minolta CM-700d) were used; and the makeup removal studies were performed on a bioskin (No 10C #WHITE).

[0164] Protocol: i. Preparation Protocol: The color of the bioskin was measured at 5 points within a 3 cm x 3 cm area using a handheld colorimeter. The color values ​​were indicated by "L", "a", and "b", where "L" represents lightness and "a" and "b" represent color elements. Next, approximately 0.015 g of liquid foundation was applied evenly to the 9 cm² area and dried with a hairdryer for 2 minutes until the surface was completely dry. Once the liquid foundation was completely dry, the color in the area of ​​the bioskin (made-up skin) with the dried foundation was measured with the colorimeter. The difference between the color value of the bare bioskin and the color of the bioskin with the dried foundation was calculated as follows (Equation i). Here, AEmax refers to the maximum value corresponding to the case where the foundation was completely removed compared to the bare bioskin.

[0165] AEmax = ^(AL^+Aa^+Ab!2) (i)

[0166] where ALi = value L for Bioskin nude - value L for Bioskin + foundation

[0167] Aai = a value for Bioskin nude - a value for Bioskin + foundation

[0168] Abi = value b for Bioskin nude - value b for Bioskin + foundation i. Removal Step: Foundation removal was studied using a frictiometer. The frictiometer parameters were set to a distance of 50 mm, a speed of 1200 mm / min, and 20 repetitions. The prepared (made-up) bioskin from the preparation step was placed and secured on the base of the frictiometer. It was positioned directly below its adapter. A cotton ball soaked in 1 g of the composition was attached to the frictiometer adapter and placed horizontally with the bioskin. The distance between them was adjusted and maintained so that they would simply adhere to each other. 100 g of external weight was placed on the adapter, and the measurement began. The base of the frictiometer was moved to the left, and the bioskin was wiped with the cotton ball to the right, as the adapter was secured in the 100 g force position. Once the frictiometer has been moved over cotton to a At a distance of 50 mm, the frictiometer was moved backward to return to its original position, and consequently, the adapter was held in place during its return. The adapter was then released, making contact with the bioskin again, and wiped by the frictiometer. This process was repeated until the bioskin had been wiped 20 times. Rinsing was performed using the same protocol. Cotton was soaked in 2 g of purified water and attached to the adapter. The bioskin was then removed and dried for 1 minute using a hairdryer. ii. Evaluation step: The completely dried bioskin was used for the evaluation step. 5 points within the area were measured and the % makeup removal (% of liquid foundation removal) was calculated as follows (Equation ii).

[0169] % makeup removal = (average AE / maximum AE)*100 (ii)

[0170] The average of 5 points was calculated by the following equation iii.

[0171] AEmean = a / (AL22+Aa22+Ab22) (iii)

[0172] where AL2 = L value for cleansed skin - L value for Bioskin+foundation

[0173] Aa2 = a value for cleansed skin - a value for Bioskin+foundation

[0174] Ab2 = value b for cleansed skin - value b for Bioskin+foundation

[0175] Observations and results: The % makeup removal data obtained for the prepared compositions are summarized in Table 2. As shown in Table 2, the makeup removal capacity in % for compositions Cl, C2, C3, C4, and C5 was > 60% (score A) and for CPI < 50% (score C). The comparative CPI compositions showed only 49% makeup removal capacity.

[0176] [Tables2] Composition Cl C2 C3 C4 C5 CPI Makeup Removal Ability 63% 65% 69% 63% 66% 49% Makeup Removal Ability Score AAAAAC

[0177] The makeup removal capacity data in % revealed that the cleansing milk compositions of the present invention were capable of effectively removing makeup. The comparative CPI composition without propylene glycol laurate exhibited minimal makeup removal, thus confirming that the composition comprising the specific components as disclosed in the present invention provided enhanced makeup removal with little or no oily effect on the skin. ADVANTAGES OF THIS INVENTION

[0178] The present invention provides a cleansing milk composition comprising propylene glycol laurate, at least one oil, at least one polymer, and water. The composition of the present invention is an effective makeup remover and also leaves less oil on the skin. Its milky white appearance, with the advantage of being a composition that can be wiped off or rinsed off, are important characteristics of the cleansing milk composition of the present invention. The non-foaming cleansing milk with less oil makes it a state-of-the-art cosmetic product for makeup removal and cleansing.

Claims

Demands

1. Cleansing milk composition comprising: a) propylene glycol laurate; b) at least one oil; c) at least one polymer; and d) water.

2. Composition according to claim 1, wherein the oil is selected from liquid hydrocarbons containing more than 16 carbon atoms, vegetable oils, liquid fatty alcohols, liquid fatty esters, or combinations thereof.

3. Composition according to claim 1, wherein the polymer is selected from an anionic associative polymer, a nonionic associative polymer, a non-associative polymer, or combinations thereof; wherein the anionic associative polymer is preferably selected from copolymers comprising at least one (meth)acrylic acid monomer, at least one Ci-C4 alkyl (meth)acrylate monomer and at least one C8-C32 alkyl (meth)acrylate monomer which is oxyethylenated, comprising from 2 to 100 mol of EO (ethylene oxide), in particular from 4 to 50 EO, or even from 10 to 40 EO; and / or in which the non-associative polymer is preferably a non-associative anionic acrylic polymer selected from a homopolymer of acrylic acid crosslinked with a pentaerythritol allylether, a sucrose allylether or a propylene allylether;and / or in which the non-ionic associative polymer is selected from celluloses or modified celluloses, preferably selected from hydroxyethylcelluloses, hydroxypropylmethylcelluloses, modified hydroxyethylcelluloses, modified hydroxypropylmethylcelluloses, or combinations thereof.;

4. Composition according to any one of the preceding claims, wherein the composition comprises at least one polyol selected from hydrocarbon compounds comprising 2 to 30 hydroxyl groups, more preferably 2 to 10 hydroxyl groups, and better 2 to 3 hydroxyl groups.

5. Composition according to any one of the preceding claims, wherein propylene glycol laurate is in an amount from 1 to 15% by weight, and preferably from 1.5 to 10% by weight, relative to the total weight of the composition; and / or wherein the polymer is in an amount from 0.01 to 10% by weight, and preferably from 0.1 to 5% by weight, relative to the total weight of the composition; and / or wherein the oil is in an amount from 1 to 12% by weight, and preferably from 2 to 12% by weight, relative to the total weight of the composition; and / or wherein the water is in an amount from 10 to 90% by weight, and preferably from 20 to 80% by weight, relative to the total weight of the composition.

6. Composition according to any one of the preceding claims, wherein the composition comprises at least one additive selected from a pH correcting agent, a preservative, a perfume, skin actives, fillers, or combinations thereof.

7. Composition according to any one of the preceding claims, wherein the composition is non-foaming or low-foaming.

8. Composition according to any one of the preceding claims, wherein the composition removes makeup from a keratinous surface.

9. A method for cleaning a keratinous surface, the method comprising applying the composition according to any one of the preceding claims to the keratinous surface.

10. Non-therapeutic makeup removal method, the method comprising applying the composition according to any one of the preceding claims to a made-up keratinous surface and rinsing to remove the makeup.