MXPA97001767A - Topical composition clear spray for care of the skin with insoluble perfume in a - Google Patents

Abstract

Aqueous clear, thick, perfume-containing aqueous compositions are provided, which comprise: (a) an aqueous hydrogel which comprises from about 0.1% to about 10% by weight of a gel-forming polymeric gelling agent, calculated on the basis of weight of the dry gelling polymeric agent, (b) from about 0.1% to about 15% by weight, of a nonionic surfactant, (c) from about 0.05% to about 5%, by weight, of insoluble perfume in water; and (d) from about 50% to about 99.75%, by weight, of water, wherein said composition has a viscosity at a temperature of 25 ° C of at least about 4,000 centipoise, and contains a sufficient amount of said nonionic surfactant to provide said perfume in a solubilized form, whereby said composition is

Description

TOPICAL COMPOSITION CLEAR SPRAY FOR CARE OF THE SKIN WITH INSOLUBLE PERFUME IN WATER BACKGROUND OF THE INVENTION Field of the Invention l pr senle i ven * I? N ~, e refers to a topical topic for the skin. More parí j t ul < • > rmeul and the reqßntp ínverifiún t - * re f r -? 're cii jitrñir onfj topical% K, for ((TIFIA or skin tnf rvuja nt i on i nal lt rimμuñ 301 i's t ic. 1 at as, Antecedents of the Invention An ampl i vat l .Jad o ((J idμo i. Innm for the (used e- »the p olol a-t ll na ns' i J J > amen to obtain benefits i > < osm li ros and / or inédi I, I HII type-, and jempl ai -i dp said i ompo j J ones i nt 1 uence < mpo it ions acondii itmadoras skin, (omposjt i ( i? '5? dfi II GD t ilpi', perfumes and tones, after-affinity and skin-renewing ompnsiiiins, in many of these types, is, ,? h1 that the ommosation ? C? have a pleasant picture or can be identi fi ed in any way, which can be used by people who use or keep the com putation. Fw I heard, ros c asos, it's desirable to use a compound that oi ulhf? the odor in ve / of, or the other agents of fraijant u. Pn mut of these ? r > (umpn H umes, tale-. too 1 or <? o? n.- > \ I? V after shaving, to posi ci one.- &perfumes &odor, a pleasant and unique smell, in fact, it may be a "?? de de de om om om om om om om om om om M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M M odors, I have a tontemde of compounds i rr.t) Iul> I e «> in ajua» 'i It may also be desirable that these products are thick, such as in the form of a gel , so that the product is less thin and leathery, is easy to apply to the skin, whether it is athletic or suspends other active ingredients (for example, skin conditioners) or the product itself 1 »'viscosity that can be compared < an other products »c nvenci nals of the same type. Additional benefits may include an improved sensation in the μie and the stability of other components in the μtrietr to. A wide variety of thickeners have been used in the area of topical compositions for the care of the skin, including, for example, hydroxy vinyl polymers, homopoly (acrylic-bonded polymers). In the same way, an alkyl ether of pentaer itr ol and an ether of sucrose, <arbo: <i> and elulose, such as met i le the ul sa hi drnx i proμ 1 o, < ro rit 1 in, silicates ',' < • "Aluminum and aluminum magnesium silicates, di- and ono- these are those of ethylene glycol, etc. Of these, the use of crosslinked and crosslinked polymers is, preferably, area of perfumed composi tions for skin care. These volume polymers are generally found in "" * "Skin care products, we refer to the art co or polimwrc" ca rbomero ", according t the f! O * tmet ic, Toiletpes and Cosmetiis Assotiation < () IFA).

It is also desirable to produce thick areas for application to the skin, which contain perfume. F.s is eec ectly eeable to form a (omf) os? Cion that sr- * thickened ion a polymer of acrylic acid linked < ruzarío, r > since it provides highly desirable properties I take vehicles for thick topical formulations for skin care. In the holder, for example, these polymers form gels, the ends are easily dissolved by contacting the electrolytes of the surface of the skin, transforming in this way, from a gel, into a gel. liquid that can be spread easily, to be aesthetically pleasing * and di- ti- 1 bui rse in an equitable manner on the surface of the skin, Rip however, it has been found that very difficult to form aqueous solutions containing both water-insoluble perfume and T) thomers of the po bomer, even in the essence of e ffective e. Therefore, it is an object of the present invention to provide ompos c i one *, thick, "laras" and perfumed to care for the skin. In particular, it is an object of the present invention to provide a composition, which contains both, oil, and insoluble smoke in water and a thickener while, still, it is still in the water. It is another object of the present invention to provide a process of fabricating 11 skin-care products, which comply with the foregoing objects, and other benefits that can be explained in the foregoing. The present description, approved by the experts in the art, can be provided according to the present invention, which will be described as "m".; N, ^ _ All, |) Orcenla is in the present description are by weight of the tomoso ion unless c? Ue? Uc? C? I? E otherwise. "> All proportions, -> on weight or weight, unless otherwise specified, all percentages, pro ucts and levels of ingredients to which we refer in the present description they are filled with the actual amount of the ingredient, and they do not include -olven, woodcutters, or other 1 <l materials as long as the input can be combined, as in the productions that are In the market, unless otherwise specified, the present invention may comprise, consist of, or consist essentially of, the essential elements described in the foregoing. 1st > the present of r i pt ion, as well as of any of the preferred ingredients,? opt i ona I is that they are also c \ ^ > (Rituals in the present disclosure.) Naty the term in the present invention means that it will be interpreted as being to exclude the use or presence of other components or steps, of the process.

'C > except if it is specified in that sense, SUMMARY OF THE INVENTION The present invention is based on an aqueous, thick, thick composition containing insoluble water perfume, ["> suitable for topical application to the skin." The compositions of the present invention include a water-insoluble, water-insoluble sample, a suf? cient amount of emulsifier. nonionic or to solubilize the perfume in the composition and a polyfoaming agent of the liquefied formaclor of hplrogel lavi -, the particulars of the compositions of the present invention, is not Hira, although for purposes of the present invention, the components must '"> be thickened-, your fiction in fear so that you have a viscosity of 'I lied-, Approximately 4,000 f utipoises at a temperature of 2 °:> degrees ('!, More specifically, The compositions of the present invention may be of aqueous, aqueous I thick, clear with content of perfume, which include: (a) An aqueous hydrogel comprising from about 0.1 * 4 to about 1 * 4, by weight, of a hydrophilic polymerizing agent, hydrogel form, calculated on a dry weight basis iiey) agent μolimépco axis I ific ante; I I (b) from approximately 0.1 * / * to approximately 1 WA per pe--. , of a south fat not so much ionic; (r.) from about 0"or > '? up to about 5% by weight of perfume and water soluble; and < d) Approximately < at 5th *? until approximately 99.73 * 4, pr > r weight, tle agu; wherein said composition has: a viscosity at a temperature of? r3ß V, of at least 4,000 c enl i fien ses; and it contains a capacity for its ionic (Je d i < ho sur faciele nt) ion to provide such a smoke in a very bright sunlight, so that it has been posited. The present invention, as well as various optional and preferred modali ties of the same, would be more detailed in terms of continuity.

DETAILED DESCRIPTION OF THE INVENTION Polymeric Salifying Agent Hydrochloride r > The compositions will comprise an aqueous gel formed from a highly absorbent hydrogel-forming agent. Will the components have a content of from about 1% to about 10%? by 'weight of the < or posi on, preferably from approximately the U 0.2.% Up to approximately "" > * /, preferably preferably from 0., V? up to about 1 * / *, of said palimépco gelifying hydrogel-forming gel agent, calculated based on c- * l hedge weight of said polimépco agent gelificate hydrogel formachlor. 1 The polymeric polymethylating agent hypoallergenic polyamide of the present invention, highly absorbent in water, and generally capable of absorbing at least about 40 g of water on a per gram basis of gel agent. fricative, preferably at least appro priately 60 / Q »more preferably at ? .a ropes RO g / g. The absorption rate can be determined as it will be depleted later. Cut tea bags Dexter tt 1234T sel lab les rum heat, in strips & cm? 1? t m, fold them along the elbow shaft and seal with heat from the three open 3 a ? 5 so that the inner surfaces of the seals are approximately "." < > up to 5.0 mm from the end of the tea bag. Place approximately. (Test "WNBt" I "wet network! , heavy dry, in tondlc? o ?? ev, - environment) of the agent μoli épco gel i fie ante for-madnr de hitlrogel inside the t bag and heat seal the end that remained unsealed-. Prepare a blank (a vacuum bag) for each sample. Fl agent * H pol mépco gel i fu ante debe - >It was well mixed immediately before the tea bags were poured. Maintain one of the tea bags containing the polymerizing gelling agent in the hoprootal position and equitably distribute the effective liquid gel agent throughout the bag. 1 * Let stand each (He tea bags (including white) have zontalmente in \ u \ re \ jpienie of 7. rm depth containing water is exu rada and hold them on the upper surface of the water during a minute, allowing the surface to be stored, tea bags, submerge each of the bags 1 tea ri for minutes, remove them from the water, and dry! as hung for five minutes. Peel one of the wet tea bags and record the grams weights of the sample wet tea bag < WW) and wet targets < ? -,), Calculate the Absorbing Capacity, as follows? 0"" <Wto + W, Absorbent Capacity <g / g> = • W, > The hydrogel is the present composition must have a level of water absorbed so that the composition is < The agent and the gel-forming agent for the purpose In dr go! have the same appearance as a gel < l ro, in ve- * of a particulate material that is not < laro. For the purposes of the present invention, the meaning of an anchorage of approximately 1. Turbide effluent units. (UNT) or 1 smaller, preferably in addition to oxidized. tle 17 UNT or less, more preferably of 1Ü> UNI or menr, »n a temperature tic * '' Ti * 'C. Fn general, the turbi er for most of the formulations of the present invention * i ou ser-a tle apr-ox i 5ly LINT (at a temperature of T "") "O or mayen-, erras general being of * 1f approximately 10 UNT or greater, although no attempt is made to reduce the levels below lINT. The clarity is edie using a Un di metro which gives the signal n fel omét r-i c a < your average diameter of 90 * ispersed), such as a Turbí d ímetro Hach Ralto / XR (Harh Campapy, loveland, Colorado, F) or a turb i ci J e tt-t) Orb * o ~ 1s Hell e (Orbwc or An l yin al Systems, lm., Fa e ngeial e, NY, USA) or equivalent, cated to e, standard ffn-irta. ' i n. Fl standard form. ' Is it also known in the field and is also stipulated by the American Public Health Ass? iation (APHA) in Standard Methods for the FVam i on of Water and Wastewater, 18a. ? or edition, 199 ?, Chapter?, μá i na. 11. The polymeric hydrolymer-forming material, when in its wet form prior to its incorporation into the compositions, will generally have the form of particles or fibers. The particles will preferably have a size of ? r > average particle (meter, or equivalent meter 3 in te-1 in the case of particles that are not spherical) of from approximately 5 to approximately no more, preferably from approximately up to approximately 60 meters, more preferably » Do not forget to add up to about 30 microns. The polymeric fibrous cementing agent for hydroejelm -r ee e ement has diameters (or equivalent diameters in the form of fibr -, which *, not in round) from approximately 1.5 to approximately 10 microns, preferably from about 1 T> to about 50 myrrhs, and lengths from about 0.1 mm to about f> mm, more preferably from about a pound. 1 '0. m until aproadamente? mm. It is important that particles or fibers smaller or smaller can be used, although they are not efficient, since larger particles or fibers can produce a granular sensation. or children similar to the granules in the projection, and 1 is particles-, smaller can t '? result in 'I f cul tacles in the proc sami ent. If particles or fiber are used, the improvement of the aesthetics of the finished product can be obtained by the corners of the compositions or other oper- ations. -analions of mezs laclo in ante til pro sami nto of the c omposi ione. In general, the materials of the polymeric gel agent are in the presence of the substance supplier of the substance.; are polymers with at least partially c-shaped bonds, prepared from polyamide monomers. , unsaturated that contain acids, which are soluble in water, or are dissolved in the hydrolysis. These include c ompu «« to «ontically and insatur-adus that are n at least one I '< radical hi r-of i 311 a, i ni luiendo. For the most part, there are at least one double olefinic bond of carbon-borne carbon dioxide and anhydrides. With respect to these monomers, solve it in water, US means that the monomer-? it is soluble in water desjom a a at a temperature of? C > ° C at a level of 1 or less 0.2%, preferably at least 1.0%. Fn the μol imen. 'ion, l units manomepra-, > As described above, they will be from about 50% by weight to about 99.99% by weight of moles, more preferably from about 1 to 99.99% by < slow of moles! Ge polymeric agent material! i ficante (base and weight of dry polymer). With e! The object of producing the ionic polymeric material, which is the former of the hitrogel, can also be used for more different types of monomers, ie monomers, which have an acidic group described above. Exemplary types of said acidic groups and other hydrophilic groups include oarbaxyl groups, anhydrocarboxylic acid anhydride, sulfuryl, sulfonyl acid, sulphonic acid salt, hydroxyl group, ether, amide, amide, and ammonium salt groups. Polymeric gel agents which are suitable for use in the present invention are well-known in the art, and are described, for example, in the Patent? R > American No. 4.07 > , AÍVI granted to Masuda and associates. sides, issued on February 28, 19 / B, US Pat. No. 4,067,817, issued to Westerman, issued December 13, 1977; the Patent Fsi doun i dense No. 4,786,087, granted to Tsubal i moto and asex lado, issued on 7 ?? August 1981; the Fstadouní Patent dense No. r?, 061,7r > 9, granted to Roldman and associates, issued on "9 of He tubro cié 1991 and US Patent No. 3, 6r > 4,039 otor-gatla to Brandt and associates, issued on 7/1 of M r / o of 19B7 and the State Patent teach that it was returned from the same RF-4,6, and on April 1, 1988, all of them incorporated in the present description in its entirety, c r e-efer The fibrous polymeric agents, eg, hydrogel-forming agents, are described in Patent No. 5,731,067, issued to le-lhac, issued by the State Department. 1988, Patent F-4,243,744, issued to the law, issued May 1, 19R, United States Patent No. 4,813,945, issued to I e-ha, on March 21 from 1989, the Patent Fs t -itloun i dense No. 4,880,868 granted to l -hhac, issued < On November 14, 1951, the State Patent No. 4,897,533 granted to Le-thac, issued on January 9, 1990, to US Pat. No. 1, 076, 784 granted. to I e-Khac, issued or cal 7D of Tumo 1991, Patent Fstadoum dense No. 5,079,306 granted to le -.-- Khac, f ** m? ? cla el / de * l-neio dc-- > 1997, United States Patent No. 0, 1, 46r.? , granted to le-lhac, issued on April 29, 1997, Patent No. 4,861,539, issued to Alien, Far-r-er and Flesher, issued on August 79, 1989, and the Patent Fsl adoun i dense No. 4,967,177, granted to Alien, F? and Flesher-, issued on October 9, 1990, to the eolies incorporated into the present description in its entirety, as a reference. Examples of suitable water-soluble monoorers are the following; 1. Monomers that contain carbohydrate groups (which contain carbohydrate 11): mono- or poly-carboxylic acids identified as monoelemic, such as blunt (meta) acr-i 1 ico (signifies ac ectio n ac e rio n or ac i tio r.) In the past similar notes are used) acid malenco, fumaric acid, acid, acid, acid heel ico, átjeJo and itracónón, acid Intar-boxi 'et i 3 enn y á? i do et a > r i 1 i < or; 7. Monc'imc-M-os that have an anhydride group of acid arboxy 1 apric acid aphidr i ros pol i < a r-bt > , < i 1 i unsaturated mannoeti 1, such as alead anhydride; 3. Monomers that contain salt of acid t arbo < i r i r g Water-soluble salts (alkali metal salts, ammonium salts, amine salts, etc.) of mono- or polyhydroxy-unsaturated monoethoxylactants such as (net) ac ri beats. of sodium, (me la) acr-i 1 a to tr i i 1 am i na, (orela) ac n 1 a ko lie tnetanol a i na, maléate.) de * sodium malea to de metí lamí n l; or 4. Monomers that contain sulphonic acid groups: vini acids theirs! phytoses at i phytos or aromatics (such as vini acid 1 osul fóni ri; ai sulon phonite, once virile 1 phonic toluene, acid sulphonic acid), acids (goal) a > -ri 11 eo sul fi'in ic fis f ilales such as (me la) t a ri of op f op-op 11 o, acid 7 - h? dr o¡ i- V (meta) at n I ox i propi the sulphonic, AcidcD 2-aci J «mi rio-7-mßt i 1 profiano« l phonic J | 5. Monomers containing sulphonic acid groups; alkali metal monomers, ammonium salts, amine salts of monomers containing sulphonic acid groups, such as those discussed above. 6. Monomers containing inorganic groups hydro-iloj alc holes *) unsaturated monoet i 1 nie riales as alcohol (meta) alilicoü, ethers') é-- > ln the case of polyols and monoether monocarboxylic acids (glycols alkylene), glycerol, polyols 10x1 alkyl polyols), such a (meta) atroylate hydrocarbon, meta) hr-ox acroplate μropy 1, or, glycol (meta) acnlate < Tethylene, mono (meta) ether 1 to 1 i e of gl? > ol pol i (ox i et 11 ene oxy prop i le) (in the? u lf »s the hydroxyl groups can be etherified or esterified). 7. Monomers containing amide groups: (meta) ac lamide, (meta) ac i lamides N-alkyl (such as N-s met la la n 1 amide, H-hoi 1 i acr- 11 ami a tia) , amide (meta) ae ri lo N, N-dialkyl (such romo N, N ~ -di met i lacn 1 amida, N, N'-d? -n- prop i lac ri 1 without nía), (meta) ac ri lamidas N- hi drox ia J qui lo L "such is like (meta) at il ami a N-metilol (meta) ac ri lamida H- hidrox íet i! oí, (meta) acri lamidas N, Nt rp cJro To whom ("such ces (goal) acri 1 acn gives N, N-1 1 1 1 x 1x lol, vinyl keys (such as N-come 11 p 1 rt ol i dona); 8. Munomers containing amino groups: esters containing amino groups (for example, steres d to which the ino lt | tu lo, ter cl 1 hi d ox 1 to Iqui lamí uo lqui 3 o, esters mor f? L 1 noal qui I, ele) de * ác gone nono-- or di-t arbox i 11 unsaturated monoet 11 éru carotene such c orne (meta) acnlata di et i laminoet 1! or, (me * ta) ac-layl cl 1 et 11 a inoet 1 lo, (meta) 11 acrylate morpholine i noel j 1, fumarate dimethyl aminoethyloxy, vinyl heterocyclic compounds as pyrilanes vinyl (for example, p ir-id ina 7-v ue, or ir id id 4-v n n, v ir id id N-vinyl), imidazole Nv? n? lo]; and '"> 9. Monomers, which contain groups of quaternary ammonium groups: N, N, N-tnal and N-1-N-) meta) acp loi 1 ox such a lam to phthale or N-chloride. , N, N ~ ti met i 1 -N- (eta) ae ri loi lox ie 11 lamonium, chlor-uro of N, N, N- tp et i 1-N- (meta) acr 11 oi 1 x let i 1 oni or, chloride e 2-h? Drox i -3- (meta) 1 < acn loi 3 ox íprop 11 tr-imelil a ouiol, and 1 a - > Menthomers mentioned in the specification of British Patent No. 1,034,796. Suitable monomers, which are converted into water-soluble by hydrolysis, for use in the present invention in VC-γ, or in conjunction with water-soluble monomers in water. they include monoetherically-unsaturated compounds having at least one hydrolysable group, such as ester and nitrile groups, said moieties having an ester group include, for example, lower alkyl esters. Cl to C3) of carboxylic acids and mixtures of vitamins and minerals, such as "t < (meta) arn lato motile, (and í,) acr-ilato ethyl and (meta) acplato 2-et i 1 hex i lo; and esleie, of ale holes i nsa turados monoet i lénic amerite r es de vinyl, ester (meta), -alilic, etc.!, such as myo acetate and (meta) alate acetate, monomers containing suitable nttnlo groups include 75 (goal) acr-i loni tr i 3 o. Preferred monomers include carboxylic acid monomers, or anhydrides or salts, of the same. The monomers are preferentially preferred, they are acrylated and arid, .tc- * tae. r-í 11 e; o and anhi í i o-, and -. them or the same. Acrylic plating is most preferred for the preparation of the liquid polymeric agent material. Although at least 50% by weight of the composition of the hydrogel polymer of the present invention, they should be prepared in part from monomers containing acidic groups, in order to remove them. Hygrogel-containing polymer compositions of the present invention, monomers which are not "(formerly" neutralised) may also be used. Said non-acidic onos can include, for example, soluble or non-aqueous soluble esters of the monomers containing the aforementioned acids, as well as monomers which do not contain carboxylic acid sulfonic acid groups. Therefore, optional non-acidic monomers may include, for example, moieties containing carboxylate or sulphonic acid esters, ertonomers which nonetheless contain lucylxture groups, ennomers containing groups amide, monomers containing group ", monomers, monomers containing nitrile groups, and monomers which bind with quaternary ammonium groups These non-acid monosaccharides are materials which are well-known and selected. They will be referred to in great detail * in, for example, US Pat. No. 4,076,663 issued to Masucia et al., issued on February 78 tic * 1978 and in United States Patent No. 4,067,817, issued to Westerman, issued on. 13 of l)? Lember * of 1977, both of which have already been mentioned in the present description as reference 8, are not present, said monomers have not been removed, they have been readjusted. generically only until the μunlo in which, ante-i of the neutr ization, no more than approxi- At least 5% of the moles of the polymer compositions of the present invention are prepared from said monomer, not e? gone. In the hydr-oge, the omnipotent polymelanic agent, formed by monomers containing unsaturated aggregates, can be developed in other types of polymer, plastic, t thimo starch ocl ul sa. Suitable starches include, for example, natural starches, starch, sweet potato starch, potato starch, wheat starch, starch > ^ a nía i- ', rice starch, starch and tapioca starches, and processed or modified starches such as alpha starch, trina starch, oxy starch, starch, aluminum starch, starch alkyl ether The starch, starch, starch, starch, starch and starch. Starch, starch c. ianoet i lo-eteri f i caio and those if my 1 ares. Suitable celluloses include, for example, celluloses obtained from wood, leaf, stems, trunks, seeds and the like; and modified celluloses such as ethyl cellulose ethanol, cellulose of organic acid, cellulose or cellulose, hydroxyl cellulose, and similar products, the developed starch materials of this type They are the ones that are preferred for the first time in the next year.

I r Fn cje- * nc- -a 1, the μe »-, or molecular (average mass) of the base polymer used μar -'- t prepare * the hydrogel-forming material, it will therefore be approximately 1,000, preferably greater than approximately 1?, 00 < > . Regardless of the nature of the basic components of the polymer of I - agents, μo3 meec ge ge! i f i cantes trainers of ludroge! used in the compositions of the present invention, said materials will be linked from cross-linking, the agents tie in < Suitable coatings are well known in the art, and include, for example, (1) tomes that have at least two double bonds - polyamory; (7) compounds having at least one double polymeric bond and at least one functional group with the tic * 3 monomer containing acid; (3) compounds having at least two functional groups reactive with the acid-containing monomer material; and (4) poly metal alloy compounds, which can form cross ionic bonds. Cross-linking agents having at least two double bonds, ie, i-i-i-i-ab, include di- or polyvinyl compounds (i) such as d i v i n i 1 has ene and d i vini 1 tol ene; (11) di- or polyether mono- or poly-arboxylic acids with polyols including, for example, di- or tri-acrylic acid esters of palols such as toluene and full, opaline trimethylol, glycerin or glycol polyol I 1; (iii) bisae n 1 m das such as N, N-met i! enob sacr-i 1 amide; (iv) esters and materials that can be obtained by means of polymerization with monomers containing hydrophilic bonds; (v) étere-, di- or poli- aillo de palióles; (vi) di- or poly-allyl steres of pal-carboxylic acids such as phthalate chalidol, adipate diallyl and the like; (vil) ntere »-, of mono- and poly-1-valent acids unsaturated with mono- to 1-i-1 or citicolines such as monoalicylic ester of acid-tertiary acid. yin o! μ 3 i et i 1 ene; and (v? > amine di- or tn-allyl) The binding agents having at least one double polymeric bond and at least one furbonate group reactive with the monomer material which contain acid include N-methylol acyl lactide, acnlate and glycid and the like, and the appropriate agent having the at least two functional groups reactive with The material of the anion containing substance includes glyoxa, polyols such as glitol et full, μol sheets t-ile-, such as alkylene alkali (for example, diamine olene), μol amines, μol i al ui] ene, pol Ieptics, di- or poly-glycolic esters, and the like, bonding agents - * suitable for the adequate ivalent metal, which can be formed in ionic form. These include, but are not limited to, nodules, hydroxides, and salts, weak elements (eg, carbonate, acetate, and the like) and alkaline earth metals (eg, cal- IO, magne io) and, i nc, by adding, for example, oxide of t a 1 c and o tli c e the t tle z i nc. The agents cié- * enlac < grazed by mu. The abovementioned documents will be described in greater detail in the Patent No. 4, 76, 663 of Fstadouni issued to M anida and associates, issued on February 2, 1970, inerawn to the present descr-ipci? n COCHO refereucía. The preferred crosslinking agents are the mono- or polycarboxylic acid diols or mono- or polyhydric carboxylic acids, the isomers, the amides and the amines di or t-a-lyl. The agents have a special relationship with you, especially at the same time. on M, N '-met i 3 euob i sac r i lamida, tr-i acr'i 3 ato tr-imeti lol μropano and amint) Ir-i-al ilo. The binding agent will usually be contacted from approximately n.OOi. μ i > read 'l mole up to 5 percent mole of the material μol iment trainer tic * hiclr? resultant gel. More generally, enlat e <agent; The agent will constitute from 0.01 percent on the white side to 3 percent of the triol of the micropolor agent or gel if the hydrogel former used in the present invention. The former developer of the present I nve-> n> e> eta link *) t ruradn lor what is lying for him, however, the graphic of the It should be enough 4 l io i oeno for the resulting polymer to exhi at a glass transition temperature (Tg) below 140 ° C. Preferably the polymer does not have a Tq below apr-ox imadamen le 150 ° C, more prêtée below less than approximately 160", and even if it is not preferable not less than approximately 0", and even more preferably not t? * a Tg prior to the deposition of the polymer in temperatures of at least 300 ° C tt crtayors. to explore differential ion (CFD) conducted in a temperature range of 2O.0"C / minut? with 3mg or 3mg of water. »» »Kl Tg« «ral on the side t.umo» l tip ftwtJia erttr-e the presentation of the nit lal and presenting it at the end of the heat flow change c rrespont to the transition to glass on the graphical ele- * c appeller of cooling uTD. The use of the CED to determine the Tg c »-" > well <onotido in the art, and it is B. Dassel and MP HiVifco in "Use of D ^ C to Dbtain Aexurate Thermodynami and I inetu Data", Amer-icart I now tory, Fuero 1994, pages 14 to 19, and by B. Wunderlich in Thermal An lys de Aradecnie Pr-e ~, s, was., 1990. cross-coated polymers slightly absorbent, such as polymers, which are referred to in the skin care industry as "e.absorbers" in the I) nd HTFA Cosmetic Tngred Dictionary lenses have lower levels cross-linking than the polymers of the present invention While these polymers are affective thickeners and are generally used in topical compositions for a good effect, or, they would not produce chemical compositions that contain insolubles in water, as those obtained in accordance with the present invention. The polymeric polymer of the present invention is preferably used in its partially neutral form. Pair? For the purposes of the present invention, materials or materials considered to be partially neutralized by at least 75 μm of the moles, and preferably at least 50 mole percent of the monomers used to form the polymer, they are the monomers that contain acid groups, which have been neutrized with a base. Cations and suitable neutralizing agents include hydroxides, and alkali metal and alkaline earth metal (eg, QH, NaDH), aconium, substi tuted ammonium, and amines such as ammonium alcohols ( for example, 7 ~ a? no-7-met i 1-1, 3- propanediol, i-alanol ai na, and 7-aen? no-7-met 11-1-por-panol). This 5 percentage of onómet or • > Totals used, those which are manome that have neutralized groups, we referred to in the present description as the "degree of neutralization". The neutralization rate will not oxidize preferably from 98%, the materials of the polymeric agent ge! The hydragel pharmacist can be prepared by reactivating the monomers and the cross-linked agents, taking those described above, by means of specialized techniques. The procedures for the synthesis of the polymeric gelling agent formator tie hitirogel. The prior art is well known in the art and is also available in US Patents NCJS. 4,654,039, 4,286,087 and, 40.70 to which we referred above. the agents μrilimeris ge! Ifie former formals of suitable hydrogel are eaten by the producers, Hoechst Ce lish Corporation, Portsmoulh, VA, FU (SanWet ™ Superabsorbent Polymer), Nippon Hhotubaí, Tapan (Aqualic ™), and Dow Chemical Company. , Midland, MT, FUÁ (Dt-y TechTM).

'Water-Insoluble Perfume The breakthroughs of this invention will comprise from about the O.O.sub.2 to about 5% by weight of a water-soluble perfume, preferably from approx. ] 0.05% up to approximately 3%, more preferably do-itie approx i maelameut and 0.1% ttasta approximately 1% .The term "per-fume1? n-» oluble "means that * the perfume '") forms a distinct phase in water (lev, united at a temperature of 25 ° C in the absence of a surfactant or other sol ubi 1. The perfumes used in the present invention, in general, they separate to form a different phase or form turbid ion in the tlesi oui zacl water, at a temperature of 75 ° C, in a concentration of 1.0% by weight) of the perfume, in wherein said turbid solutión has a greater turbidity of IJNT than was previously described. The term "per-fume" means a volatile, fragrant component of a or or more per-fume active compounds, the child is a *. t < a pleasant one, or another desirable mood, in the context of the lens, the atmosphere, or the tone is used to hide odors. F] per-fume contains compound odorous perfume ingredients insoluble in water and may also include ingredients such as solvent diluents for solid perfume ingreciients, and fixatives, etc. or perfumes in the present invention, in general, are liquid in the ambient temperature and -strict for a point. of flastt from about 10 ° to about 170 ° C, plus genora 1 from approximately 75 ° C to approximately 95 ° C (determined in accordance with) 5 Standard AñTM D-56 O.e .) Standar Test Method fot- Flash Point by TAg Closed Tester). The active perfume compounds are usually inorganized in the elemental components in liquid form, but they can also be solids (such as different alkaline fragrances). They are on the other ingredients of other perfume ingredients, as explained above, in addition to the perfume compositions at < 1 ivo, the μe smoke < In addition, the invention may also include additional materials, listeners, solvent ingredients for solid perfume and fixatives, etc. Diaries may have, or may not have, their own aroma and, up to the point where they have it, they are classified as p-compounds. active smoke, the examples of the 11 enemies and the solvents i nc! uy »n lc holes (for example, ethyl alcohol, tertiary alcohol, fluoride < l i μrop 1 ene, etc.) and liquid substances and esters of I. i clt or arbitrator (for example, benzyl benzoate and other hydrocarbons and esters described above). The fixatives are in redi ntes that prolong the durable quality tJel μr-n smoke during the use and can do so modifying the general volatility of the perfume component. Some fixers can function as if they were active perfume, while others do not. To the extent that a particular ingredient performs pumice fume, it will be considered a composite of artificial perfume. Examples of the ingredients include perfume ingredients, which will be described further below. A wide range of active smoke compounds are described in Perfumes, Flav? Rs < i. \ > you Chemic ls, Volumes I and 11 of 8. Arctander, Aurthor, Monte 1 a i r-, NJ, index Me fc, 8a.

Edition, Mer! ro. , Inc., Raln-ia, NJ, and r ~ n Handbool * of Perfumes and Flavors, Se ond i ni, Chemic al Publ ishing Co. , 1 nt., New Yort, NY 1 90 (ISBN) 0-R7 6-O, 4-1). The μer fume típic or c omprender a μ I ura 1 it has 5 individual compounds of μer f wiv acivo, although it can con -,? S? Es essentially tic- »a single ingredient of perfume. The addition of the ingredients in the component "perfume" and / or the motion of the relative levels, depending on the ingredients, is a practice that is found within a high level of the experts in «, l art. Various types of chemical compounds generally known to be used in perfumery, which include: phenolic compounds, acid essences, aldehydes; l-etonas; compounds μol ir ¡c 1 n os; esters and alcohols. Many of the 5 entries of perfume have a combination of functional groups and can be * c allegorized under two or more of the previous classes. From the point of view of the perfume preparer, it is convenient to consider the in rents of the perfume in terms of the type of flavor it imparts, rather than the particular products in which they can be classified. The perfume components of the present invention can be formulated to provide a variety of-1 odor categories, a non-exclusive list includes, wood perfumes, sweets, triethos, florals, flowers, animal species, green, musk, balsamic, chemical and peppermint. A variety of "perfume ingredients" are described below, par-a vr-ias of the categories of oi oree generally used--, together with their representative chemical categories (but not necessarily exclusive). The i ngr tl i eirt is the perfume * tie lumber will include, cedar wood oil (oil essence), oil of guayaco wood (acte de osenc ia) youona gamma (busty), oil wood of - * sandalwood (essence oil) and me il cednlona (t-etona). The ingredients of sweet perms include coliman na (busty), vanillin (4-hydroxy-3-meta-1-hydroxy aldehyde), ethyl methanol (Alkhol), phenyl. ac etalcleti gone (aldehyde), heliotropin (aldehyde), actophenone (tetona), and ci i h i d roe < > uma r i no (t e tona). The incen tives of the citrus fumes and the orange oil (ai e-tle esen i), the lemon (essence), tritrico (aldehyde), beta and il uaf ti 1 t-etona (tetona), ci lerμinil acetate (ester), aldehyde onyl (aldetido), terpineol (alcohol), and di Ip dr-om irc euol (alcohol). The invents of the floral perfumes and a variety of floral products, such as rose, lavender, jasmine and "mttguet", the ingredients of the perfume of r-bear include geranyl acetate (ester) , geran ol (alcohol), acetate and ci tron! i lo (ester), alcohol ft.'iti 1 etílic o (lcohol), alfa da ascone (busty), ball clamase one (busty), oil geranium tie (acei le e is rn? a) and ac ei le tosa natural (atei te tle-> esenc la).

The ingredients of the lavender pejrfumt include dihydro terpene acetate (ester1), ethylhexyl tertiary (tetone), lavandrt (acite of that -), lavender ("ti ei le de e", in? a), l iuaool te »tra hitlres (alcohol), I mal? ol (alc hol) and l inal acetate? (ester). The ingredients of the perfume »of Tazcnin include benzyl acetate (ester), aldehyde, butyl cycloalkyl (aldehyde), benzoate methyl (ester), natural spirit of the ji mlp (" ac i te de es nr i-i) aztnonato ethyl cylinder (ester-) the i ngr-ed i ntes of perfume - »tie" mugitet "i nc luyt-ín aldetndo de < go to en a 1 debí ció), sal ic i tato bene íl to (ester), h idr o. ici I ronol or I (alc hol), oxac eta 1 clohi do e »ci troné» 11 o (a 1 eti io), and aldeh ido h ielrox i lo ( aldehyde). The fruit fruity perfume in luyen buty ato 1 ~ 7-mei 1 o (ester), μropionalo of ai l cl? hexan? (ester), acetate ai to (é t et , -tllo de- et i lo (é -.-, ler), eiecalactana range (t etona), or * talat tona (t etona), uitelec lai lona (alcleh i de.), aclal or eti acetes (ester), benzaldehyde (aldehyde). The ingredients of the perfume. * Animal? npluyc »n ac tate of methyl fem lo (ester), intlol (2,3-beuznμrol e) (phenol ico), creosol (phenol ic), qui nol ina \ - > n buti lo (phenol ic o) and an rostenol (phenol i o). The ingredients have a pericum of anhydric aldehyde (aldehyde), an aniso (acetyl ester), clove oil (essential oil), eugenal (phenolic, eugenic (phenol). ico), thymyl (phenol ico), anelol (phenol co), cyclic ammonium (alcohol), and cynmic aldehyde (aldehyde). The i ngreel i of green urea-fumes include beta gamma h xenol (to 1 • ohol), bi mu, i i ro t (a 1 och), tar-lnitol di met i 1 bencico (alcohol), tr tonona de meli l he- »f) t? na (ester1), acid of cis-3-hexen? it, and galley oil (ac i e de esenc i). The ingredients of the permeate that often function as well, for example, include examples of glaxalloid (fc *? tol), iic 1 of) c * ntadec t'il i ció (phenol), I- c- »tona of l mi''que (busty), arnbret í 1 i des (phenol), tonal i o (phenol), and brasil ato de et i lorio (ési er). The ingredients of the lsámic or smoke firing balsam (ac ei te deí esenc la) b lina of entina (at ei of essence) and resinoid ele3 benzoiua (ac ei of esenc i). < * or - Ingredients of the fume quitrin or include alcohol benzyl alcohol (alcohol), glycol chpropyne (alcohol), ethanol (alcohol) and benzoate benzylitic (ester). the ingredients of the perfume of enenta include the eve c-vone (ketona), menthol (alcohol), sal ic i lato de meti lo (esler), 5 ae: e? te de pepermin (acei te tle essence), mint extract (essence oil), euc lipt (ac i te de-ensen- sia), anisi acetate (ester), rrseli l c havie ol (alcohol).

Non-ionic Surfactant < < l as < or examples of the present invention will range from approximately O. 1 * 4 ln d.a to an oximeter on 15 * /. by weight, of non-ionic surfactant, preferably from about 0.1 * 4 to about 10 * 4, more preferably from 0.5 to 4, preferably from 5 to 4. I can u-- > A non-ionic surfactant or a combination of non-ionic surfactants. The amount of non-ionic or used surfing must be sufficient for the sun to locate the perfume while it is possible, so that formulations are prepared. The term "clar-a" is defined, the J and as described above. Therefore, mere emulsions that are characterized by opac or transparent opacities, are not included in the Sere i nvenc ion. Although in theory, the perfume has the present invention, it is still "emul s i f i c acio", the droplets of »perfume, even its f i < In short, the composition has a long-term appearance, as would be a "sun ion" in the theoretical sense. The term "scsluci? N" for purposes of The present invention is defined as meaning that these words can be used in a wide variety of non-ionic, non-ionic ways. You can also use a wide variety of non-ionic cations for the particular compositions-es. In general, the level of surfactant used must be higher than the critical micelle concentration of the composition, the object is to locate the perfume and produce a clear proclutte. The specific quality of any specific sur- face will depend on the chemical types used, the perfume materials used, the faithful perfume level, the chemical type, and the amount of fi xed material. - 1 i í i ico (Hl) of I sur fat tante- *, the presence of electrolytes in the composition, and other factors as well as those well known to the art experts. The choice of surfactant or ionic treatment should be such that the lipophilic portion of the non-ionic sur-fat lanle is compatible with the per-fume and so that the surfactant forms a mi-cr oemul si ón de acei e- * in water .. These surfactants:, in general, they will have an HLB ci from »aμro,. The average HLB can be calculated with the arithmetical averages of the mass of the individual components of the south 1, respectively, up to about IR, preferably from about 8 to about 15. When using loue-, dt »- >; ur-fac non-ionic laitles. The average HI.P of the total component of the non-ionic surface factor is preferably from 8 to 15 percent immedi- ately. The methods for determining the HL R and the uses of the Hl P as a guide on the solete I'm on. r i be μor example, in "Casmetics Se leuor" and Tec hnology, Second Edition, Volume of. » M. S. Balsam and Fodiard Iiagariit, 1974, John Wiley? T Sons (Ne? »York), pages tie] 5R3 to 5 < R, Coll n! and Trtterface Rpence, Volumen TI, Mill n 1 «rter, A 'ademi Prc * sss Inc., (nuw Yort), 1976, pages 437 to 435. 5 Homo will be e omμr eueh do μor experts in art, "Non-ionic surfing material for use" in the present invention will vary according to the particular chemical facets of the perfume. In general, it is preferred to use nonionic surfactants that have lypofilic or chemical types (for example, lone -, ether, and the like), which are the same as the ingredients. nte *, lipophilic in the perfume insoluble in cjti. The surface is so many a lone if they comprehend extensively the compounds produced by the opdensat ion of the groups of 1'-alkylene (of the nature of the draft, 11 c) with a compound of water. Phobic, 1 o-, which can be of ali phatic or aresatic nature, as well as other types, of sur- lalations not "M (Cynics, lo *, examples flt-1 la *, t 1a The following are suitable non-cyclic surfactants: 1. Phthaloxides of alkyl phenols, for example, the pro-tect of the alkaline phenols. only, that they contain "> an alky group" that will be delivered from a? r-c >? i? up to approximately 70 atom *, of a bonus, in configurations *, either the chain or the other branch, and on the other hand, said oxide being present in equal amounts, from * approximately 10 up to 10% at the same time. ol *, of ett. et filled by mole * of phenol alkyi. Fl sub-, l? tuyenl Alkyl in such substances can be derived from impersonal pr-cspi leno, i-i sobut i e-Mine, that label or nano, for example. 7, Surfing tanteas tie »pol i csx i et i 1 cryo derived from the ethylene cell condensation in a hydrophobic group as well as in an alkali (for example, only monomer units) or pol i csx i prop i 1 ene, oo! μr ocien lo r-esul lanío '3 a reac < ion de »csxido propileno y |) r-ocluc tos diamina eli leno, For example, are sa if c *, c omposed to c from about 40 * 4 to approximatively f-) o'4 of μol i ox i et 11 enoμor pes i and that have a molecular weight of approximately. 5.00 (5 to approximately 11,000 results of the reagent of the ethylene oxide groups with the base ItieJrofoluc onsuite of the reaction product of the diamine and the oxide and the excessive oxide, the base having a molecular weight on the order of 5 about 7,500 up to about 7,000,000. Also contemplated are the opol i or-os of the oxide block 1 to 1 etto, such as 1 css non-ionic surfing pol i (oxieli leno e o- csx i prcspi leño) and ome »ro i a 1 i zade-, under the commercial mart Pl? Romt *. < R) (BASF Wyanclolte Hor-p.) - and the mark c esmere tai Fmulg? N ", (Hent-the Hrrpora ti on ~ Fme-ry Group, Cinc innati, DH FU), such as the PP6--7- Ce lere I o- 9- Fsrtul cj in < n>, r? The * so many favorite of this type are ethers propox i 1 aeios, etoxi l dos tle alqui lo tle 013 to Cs-o, preferably of Cu »to C», _ s, more preferably * to C o * alcohols, (for example, alcohols (ethylene and eslearl? n) that t? t »nt» n an average tle from approximately 7 to approximately 4 groups of people and projects, 1? Preferably, 7, and 7, and from 7 to 12 or approximately 11 groups, preferably from the outset? 8 to approximately 1.0, more preferably approximately 9.7 > . Alc oholes ethoxy side », for example, the product of» the condensation of alc hole »*, at the f os ers that have from about R up to about 1R carbon atoms, in configuration, and be straight line or branched chain with ethylene oxide, for example, the > niidensado do c x i do eti lon? of cfw alktol which has t from approximately 10 to ? Approximately 7, "... is" of C? S? íÍÍO and filled by mole of alcohol of »« ne o, having the de-alcohol frucción de »coconut approximately the appropiately 14 atoms of alcohol 4. The oxides tic * amine tertiary to * larrea chain that » 75 correspond to the following »general formula R-jR ^ RgN wherein R * contains a t-n-alkyl, alkyl or alkyl-hydroxy alkoxy from about 15% carbon atoms, from or to about 10 per-c. ions of oxide the leno and from 0 to approximately 1 glyceryl portion, and R_s and R3 have from approximately 1 to approximately, 7 atoms, and from approximately the hydroxy group, for example, radicals, ethyl, prcspiles, hydroxyl, and i oohi dr ox i propi 3? (the arrow in the formula is a c onvene tonal ion representation of a ipolar link). Examples of suitable tertiary amine oxides to be used in the first invention include oxide of 11 -dodec-1-amine, oxi- or oli-1-di (7-h? clrox-i and i-1). amine, csx icio di et i lo 11 lamí na, enceles cli et i 1-dec i 3 amine, oxide di otil-tetratlet i 1 am i na, oxide 7,, b, 9- I p oxahep ladee i 3 cliet i 1 amine, oxide di < 7-h? drox i e * t i 3) tetr ade- and i lamí na, oxide T'- odec aox i et i 1 - dimeti lamina, oxide 7-dode? ao < ? - 7 - h? Drox i prop i 1 ti i (3- 'your di'ox i pr-csp? 1) am? na, oxide di met i Ihexaclec i 1 ami na. 5. The oxides of fo fiua lert? Ar-? of »long chain corresponding to the following * general formula: RR '"p > O Where R contains an alkyl, alkenyl or monohydroxy radical; 1 or in a range of from approximately 8 to approximately IR atoms in the length of the chain, from 0 to approximately 10 μs ions from oxide to ion and from 0 to a μm; i acme te 1 porc i n gl ie er-i! and R 'and R "are each one of the groups that either have or do not know what they have from approximately 1 to approximately 7 minutes of the arbono. A mule is a representation of an ion and a nucleus of a bond that is ipolar, examples of which are the proper oxides of sulfur are: oxide dodecyl 1 di met i 1 phosphine, cs gone tetradec i Idi rne-111 phosphine, rhodium oxide, and 1-methyl-1-ethylene oxide, oxide 3,6, 9-tr icsxa-ot tadee i 1 di mel i I fo *, fi na, oxide c et i Id i me 111 f < is fi na, c ') to do 3-dodecaox i -7 ~ hi elr oi i i o i i di < 7-ft i clr oi the i fi) fi os, or i des estean! di met i 1 fosfna, e't gone c il i 1 p'opí! fosf i na, c'txid? oleí 1 di et i 3 fi os fi na, oxide elodec i 1 cl i et i 1 phosphine, tetracyclic oxide, 3-oxide, 1-phosphorus oxide, oxido elode, i-di-op-1 phosphine, oxides odec i ldi (hy drox i met i 1) fosfirta, encelo elodee i 1 cl t (7 - hi ro-c i et i 1) phosphine, tetradec oxide 11 met t 1 - 2 ~ h? dresx i μropí 1 f os fi na, oxides tsle "»? i i fnet i 1 f fi ne, o / i tio 7-hi drox i cloder i 1 di et 11 f fi n f «sulfoxides fhalcμii The long chain that contains an alkyl radical or hydroxy to the short chain of * from * approximately 1 ha, the approximately 7 carbon atoms.

(I usually put it in) and a long fyrophobic e-na which includes alkylo, alqueni, holto < ? alc | u? or, to the cinema, they contain dt - »-, from» a «or - matlamente - * R up to approximately 70 a - year, from c - bono, from 0 to approximately 10 by. oxide eli leno and tie »~, appropriately O up to approximately 1 percent gl? < er? The examples include: its toxicity, sulfoxide, etotropic acid, sulfur, 6, 9-trioxac and 1-2-hydroxyethanol, sulfoxide dode. 1.1 motile, sulfoxide 3-hydroxy propyl 1, suH > V'ido lolrade il melilts, - > u I fox gone 3-rrtetoxy tp dec t 1 methyl, > ul 3-h ulrox i tp de »ci 1 methyl, sulfoxide 7 / - hi tiro1 '? -4" dode * t aox i bul i 1 moti le. "7, Pol i sorba cough, μor example é, I 're ele "-sacar-osa of fatty acids, Said materials are mentioned in the American Patent No., 480, 1 /), μor example or sac-sosocoat (a me :: cla ti *» é- >; teres e sac rose of a cessation acid. or, consisting mainly of mnuués teres and eat rr rl under the names romer «: ial is fie GRII I OTEN i RF R71 for- RITA and CRODERTA BL-40 for Creída). R, ls -. Ur-far laidos not lóme os de μnl isac alkyl se- * descr? Be »p in the Patent Estadouni Ense No,, 565, 647, granted to Llenado, issued on 71 tic-» Fuero tie 19R6, who have a high-tech group that "has approximately .6 to approximately." 3 < "> arbono atoms, preferably from * *, from about 10 up to approximately 16 carbon atoms and a poly saccharide, for example, a polysome, cosmic, hydrophilic group. It can hold 1 from about 1.0 to about 10, preferably from about 1.7 to about 3, even more preferably from about 1.3 to about 7.7 units, which can be removed. u-, atta c ualquie *, ac aricia t-edttt tora that contains 5 e ') 6 carbon atoms, for example, the por ions of »glucosa, galactosa and cj-? lat tosí 1 can be substi This is given by the μor-t tone-, of »gltu osi l. (Dμt i ona 1 the group h idrofób i < is connected in the-, pos itions 7-, 3-, 4-, ett:. leudes de o, lv odo a gliuosa or (jalat slab as opposed? 1 glucoside or alat tc'tsi o). The Ine ss i nlersae aria may be, for example, between the pcssie ie ' srt une.) of the additional 5 units of arid and la-, ions post 7-, 3-, 4-, and / or 6- of the units of sai anda μr-ot ed n les "Oμe i una First, there can be a chain of oxide with 3 ui 1 joining the hydrophobic portion and the portion of polyacetylene. The alkyl group can contain up to 7 groups huiro; i lo and / or the oxide chain, pol i a 3 qui 3 ene can contain up to about -10, preferably less than 5, alkylene portions. ls pol i take suitable alkyl snn octyl, noni 1 cleci lo, undec i 3 oc i 1, tptlethyl, letradecilo, pen ladee i 1 o, hexaclecles, heptadecyl and octadecyl, di-, tp-, tetra-, peota ™ and 5 hexa l ucósi dos, ga 3 ac. tessi dos, 1 ae tosidos, glucose *, fruc tosidos, fruc osas y / galae losa- ,. 9. L esters g os glirepl (PFB) cié glycol po! Let i 3 ents, are illustrated by the formula RC (p> OCHapH (nH) pH »(r) CHa.f: Htf) npH where tt is from * .de or approximately 5 up to approximately 7O0, preferably from Approximately 2? ha .la aμ? -t > x? matlamc? 100, more preferably approximately 30 to approximately 85, and RC (f)) - is where it comprises "aliphatic radicle eue- > it has from about 7 to 10 μm and a least 5 19 carbon atoms, preferably from about 9 to 17 carbon atoms, more preferably from about 11 to 14 atoms of carbon. »Carbon. Repref-t-r in the combinations of n from approximately 70 to approximately 100, with graphite esters from Ca to Clß, preferably from C12 to Ci», for miiiimi / ai ' The opposite of the "generation" of "espum." 10. Di met i 1 pesl if 1 csxanos such as oxide pol 1, which was modified, also known as "eopolies" i tic ona. These materials include the following: i i i i i i i i i loxane oxide pol i to the one modified by the following formula: R '. Yes { [0 • Yes. (CH3) 2 x (OC2H4) a - (0C3H <,) b - OR "] 3 where R is hi dre ') ge »no, a alkyl group having from 1 to approximately 17' to volume, tle c arbon, a cxr-upo alcxcx that has de 1 s until apr-oxidly 7th atom of carbon, a hydroxyl group or tr-iglie gone from C to 3.S. ,, R 'and P "are alkyl groups having 1 to up to 1 μm, 17 carbon atoms, x is an integer from 1 to approximately 100, preferably approximately 7 to 30, and is integer ds 1. until approximately 7c "), pre f eren tly-» from 7 to approximately 10; .- e, an integer of »from 1 to 6, preferably * from 7 to 4; and a and b are integers from 0 to approximately 50, preferably from 70 to 3o. the c opo! joles ele "* dimethicone are those of the formula: I t opol i oles of intel icona e» tán esc ri tos in the following * »dot tímenlos of patent *, all -» incorporated to the present desc rip inc mo refer ne The US Patent No. 4,122,079 issued to Reen and associates, issued on October 24, 1978, Patent Fsladoun t dense- "No. 4,265,878, issued on May 5," May of * 19R1; "American"., 4,471, 769 ravaged to Di xon and associates, t-* m? l on Dec. 7, 1983. I css i spol ials of »chmetitoua * that are available in the market , which are otiles on the present invention, and include the Copolymers of Buperfu le At 11 va Sil ni l (manufactured by Union Carbide »Corpora ion), the silicone co-surfers Dow Corning (Manufactured by Dow Corning Corpor tion), Copolymer of Si li cuts F-754 (fabric do μor- Wf? Si l irons Coi-f).), Rhodorsil 70646 Iquid (Fabpcatlo μor1 Rhone Poulenc, T nc.), and the Fanc orsil LTM-1 (ei i i ng of c ool iol elel i i on on) of The Fanniug Corp. (Chicago, 11, FU). 11. Surfactants which can be used in the present invention include the fatty acid amides of polyhydric or N-aikyl of C,., -,. I tt-, typical examples include the N-met i 1 gl tt aen i da of C,? Aa Clf3. Ve - *! 1 «1 ot ucrenlo WH 9,706,154 and the Patent Fstadoum dense No. 5,194,696 i nt Orporados a la pr-ese »nle cler * rr its reference. fltr-os surfac tants derived from a. otri IK luyen ls amida *. e» acid greasy pol i hi (trox i 1 N - I, I, I, I, I n the N- (3-melo? i prop i]) luc amide of »C1C? íe». I, s gl u, ami das »i» »l M-pr -opy to the Nt »?? lc> from Cía to C_.ß would be lrefetidas par-a api 11 ar i one-, a ls that * you want a pot? The url c lens, μre f r11 dr &nc l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l l Ipol i *, i 1 or ano *, with oxide polia I i 1 modified, and a * "t l -, de- lo-, themselves. They are espe- tially μe- * f ers the days. oμol lulo-, de d? me »lu ona and the ethers pr-opox i 1 atlo-, elo; 1-Alloylions, preferably in a proportion of weight from about 0.1 s 1, 0 ha- > Approximately 7.0, 1.0, more preferably at least 1, at least 0.5; 1.0 up to 1.5; 1.0.

Aoua ls comp? Sic ions < csmpr encloc n dc »sde» approximately 0% until approximately 99.75 '/ »by weight, of» water, preferably from ¡.pro - i madamenle 65 ttasta approximately 99.65' /, more pr? Of aproi; i maclameute on the 8th and, then, the first step is the 99.55V, Clear Thick Compositions The tum ostitudes of the present invention will have m \ ^ suf fi cient amount of "agent" for the correctness of the product, so that the average size of the products has an average viscosity. In this case, in a temperature of 75 75 C C, a i 4 at ((((((((((((((((((((((((((((( With a stand, the size of a bar-T tic »1,475 inches (3.65 cm) at a speed of 5.0 revol ai oues / null, in a range of inac tion of 7, m / m? n? to and being taken the medìa after  »a ¡tu 1 inai ion tie 7. inutos (μor example, 2. 0 minutes after the initiation of the agitator bar with the surface of the μr-otlur lo), or equiv lente.- ». The average viscosity p r f is from about 7000 to about J0, O00 e in t i poi, more preferably * from about 7.0 o0 to apr imadamente ,000. The ions of »the μrt» are also clear. As used in the prest-sote descripe ion, "c lar-a" means a lurbide »tle» approximately 20 IJNT or less at a temperature of 75 ß C, μre »f er get it from» a μroximately 17 IINT or less , more preferably de-api; i raised 15 UNT or less. t turb? de2 will generally be at least at least 5 UNT (25 * C), more generally at least about 10 UNT, although formulas with UNT huge do not mean they are extended. . The turbidity. "Is measured as it was» beforehand ». The molecules of the pre *, in addition, are essentially the same as the polymers of carboxylic acid, for example, polyethylene oxide. thickener agents of the type of * acid | > At the same time, other polymethics of hydrogels have a low molecular weight of 140 ° C, and are pref- erably The size of the polymer that has a T below it is approximately 15 * 0"C, plus μ ref» below »about 160 ° C, even more preferably below about 180 ° C, and even more preferably, the polymeric dumbell with lower Tg1 at 300 ° C is depleted by a high molecular weight. "esenci l ente-* l ibre" < - > ? gu? Why would any technology that would reduce the volume of the system? In order to have a definite, open-ended clarity, the broadest definition of "lurbide" defined above (70 UNI) and μr e- »f or oulemetd e-» c tta 1 qu i e-rc nity of the polymer that will clarify that the clarity is uv, it will be from the limits *, defined by the definite rider.

Optional Ingredients l s μ? C »se» nts < I occupy • > i < The purpose is to understand a wide variety of ingredients, or tonal ones. However, such optional inputs should be misleading, soluble or soluble in any other way in the formulations, so that the omposition For example, if the said component is not soluble in water, it may be solubilized by the non-ionic surfactant described herein or by oestrus surfactant. It is also possible that the solution or solubility of the solution (such a chromium is present), so that they are molded to a μr-clear nucleus. Such optional ingredients can be used, for example, for aesthetic purposes, mucosities, medicinal purposes, purposes of the skin, or fatigue of the process. The examples of the inputs *, will be described in detail below. As long as they are added, the optional ingredients must be included in the (e-, RH level »1, suf fi cient to produce the intended benefit, In general these ingredients will be added at a level of» immately 0.05% or greater1 5 depending on the efit e of »li ngreel particular ute.

Aoentes Acondicionadores Los ayente »s acond i < suitable fillers for use in the present invention? luyen l? ome. »(tantes y emol i entes.

! In general, the agents involved are inoculated at levels of approximately 30%, for example, or for the composition, μ? eferentt »me? ? fie? - up to approx i maclame »?? you- »10%. When they are aggregated to provide functional benefits, they should generally be aggregated at a level of at least about 5% approximately, preferably at least about 0.1%, with examples of ls. Soluble soluble agents include diols and triols, C3 Ce, for example, and the propylene, hexol, hexol, 1,3-di-dimethyl and pr-opane, glycol (butyl). , 1, 4 - d? Lu dro / i he / ano, triol 1, 7, -he? Ano, cjl je eprw y 1 s s i m i 1 res. Other air conditioning agents are included! other alcohols pol i h itlrox i 1 o, such > or sorbitol and sugars and starches and derivatives thereof, such as sugars and 5 alkoxy-sided starches, μor e-* eamμlc > , glucosa at 1 cote i 1 aci, at e: »vera; panthenol; a ulo hi < ? 1 uron or o; onoetancsl amine de lacl rmela; moriese tañes] arru na d * oc lamida; gl ol ol lol i ot, i 1 e- »no (PFC &) and esters PER e:» acid *, mono-fatty, di and I r iql u ér ido *, (μor- e »je» rnplo, PFIR - 14, e apr i 1 a lo / ta y) to PFR P, G1 u e '»r of 1 to 1 me» ntir as PF6-60) that they have an average degree axis ethoxi lac ton of »from? approx i madame-'itle »5 to 7no¡¡ ur ea; and guan ul i na »I css Agents at t he appropriate level and they also have soluble emollients such as isosorbide imeti lo, glycol ether propylene of butaiecl ia 1 or other *, ti i - hi cl -tsx i to c anol is of »C a í that tie» have a ntvf »l total average cié» μroμox i 1 ac. Since approximately 4 ha -, has it been approved? aprox i maclacrronle P, until apr-o; i madamen te 17 íμor t- »example, tutianodia PPR - R), and é -» e t -, cie acr - »te» s fatos tie »gl it ol pol i propí! enes (PPF-R) / gl o or I μol iel? lt »no t.R), lale» s as oleic, palmitic, stearic and lonele, which l »e * n a degree pt-omedirs of pr-opo i lac i c '> n of * of, of apr-o! from 4 to approximately 70 and an average degree of ethoxylase of approx. 5 to a maximum of 700 (for example, fatty oils PPR 10-7O / PFR 4O-IO0) or the oil-* of »lanolin PPR 17-PFB 65)" Other agents ache atedores, including insoluble emollients such as the volatile and non-volatile metal, the i on u onol eu lomel u ona and » str * os si l icones, hidro rburos, f - '»su > re-- > cjr < ¡, Or *, and lc hole »s, and the similes can also be used provided that, umμl with the l imi tes and turbidity cié- * prc ~» se »» IIVPUI.K'HI .

K) »ntfgif dw 8ffniftci, 6p And Rftfrtt» cancas Re can u »» ar a wide v a rity of »ref rescnt and agoutes materials» use »< ic n The agents of * »ensac? n i nt lt? e - n n nn, > silent tree n 1 \ r ^ • - < such as those "* described in the Patent" and "No. 4,730.6RR, granted to Rowsel 1 and associates, issued on October 7, 1980, included in the μre *, deciphering entity as reference, for example N, 7, 3- Ir11 me »1 i 1 --7 tsopr op i 1 - butauam t tía and Carboxami as p.mentano-3-N sub - &ti ti da • > I a 1 c- »scool *, which» are rilen in the Patent * Estadouni ense No. 4, 136, 163 granted to alson and associates, issued e]? ", ció Fuor-o tle 1979 , included in the present document is referred to as, for example, Ne 111 - p-mentano-3-t arboxami da. I ts-, agents of-, e-nsac i e'tn are generally used at tie levels from approximately 0.01 $ to approximately 7% μor less, preferably from approximately 1% to 0%. , 05% ha - »the oxidized to 1.0%, more preferably from approximately 0.05% to approx. 0.5%. he refreshed them ant *. They include volatile liquids that are evaporated over the liquid, therefore, in a cooling sensation. Preferred fresh csses include -!) Ethanol, alcohol isopropyl and bird! wool. The level of * said refresh *, μueele vapat to μ 1 i menle ». In general, if they are used for reflectronic purposes, they will add at levels of at least about 0.5% μcsr, preferably by at least about 1%. The maximum levels are governed by - issues μrá < your ex- and the desired degree of desire, as well as the desire to minimize the possible risk, and generally will not be more than about 40%, generally not more than about 30%. eleven Skin Renewing Agents In the case of t * t * t * t * t * t * t * t * t * t * t * t * t * t * t * t * t * t * t * t * t * t * t * t * t, they can use renewa- novice agents that can be generated in 5 levels. from »from» 0.05% up to apt o- 5% μor weight, preferably from »to μrown» >; - *! 0.1% up to about 7%. These include acid to 1-ith-11-ions, such as glycolic acid, and glutaric acid, salicylic acid, lactic acid, and other acid. 1- Additional Co-composers in the present invention may comprise a wide range of functions (including additional examples of these types of ompont- »nesses ad i cion 1 e» s i cluyen, anti-acne agents, agents for the generation of foam, antimicrobial agents, antioxydants, binders, biological additives, regulating agents, agonizing agents, c odor n »» * -, cosmetic astringents, hypotesis with osméticula, nour turing, as tn nts tlf »medicine *», anal external psy chines, axis formers » '' ('film, components tic »fragane ta, adjusters of» pH, preservatives, teclucorctants », whitening agents and pical, agents tle» fil lret - »ol ar (for example, absorbent light (iolet); solvent-, t <? 1 is like monohydric alcohols from »Ct to C * (generally at levels of from 0% to approximatively.» 75%, preferably * from »e-» l?% Up to at least 20%, more than 0% of the approximately 0% h-tsla), especially ethanol 5 ote. fifteen Other examples are not similar to these ad-tonal components, and they are used to identify and derive from them (for example), the offeror, at the Toc Ferol, Acid ret Retics, Ret i no!, re inen es, yls simi lares); polymers to help in the prop ions of the film for- mat and the ivory end of the po omy (such as the original op e) and the e sine and pi rrcsl i tlona vi ni l it, an example of- * e- * - * < omμoneitle. »is omitted by RAF Cltomit l Corpor at ion as Ganen <?) V-770); conservatives μar-a? r? anle »ne» r the authentic self-integrity of the I »compositions, ol? o =, medi i airen uis t ont id the ac né (μor e »je» mples, restire mol, adufre, ác io sal ic? lii o, e * ro troen irt na, and the similar ones), and whiteners The light (or light-emitting agent) is changing, whether or not it is being imitated, at the end of the day, at the end of the day, anti-oxidizers, chelators and semen. c uest iers 15 Manufacturing Process the e mployment of the aforementioned "e n n. ve pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden pueden Proceso Proceso Proceso Proceso Proceso Proceso Proceso Proceso Proceso Proceso C onvenc inl techniques * »-, c ouot idas e- * ?? the ar. o Pr fer tínl e» menl e, la *, c omμo -,? t? o? u- »sc onsisten ci; (a ) μr cl una una una ac ac ac ac ac ac ac ac ac ac μ μ μ μ μ μ μ μ μ μ μ μ,,,,,,,,,,,,,, - - - - - - - - - - - - - - - - - - e omμns ic 10n of »per-fume * i oluble in cough, of *, of» aμr oudamente, - > | e ") .1% ha -, 1a aμr or imadamente» 5 15% by total weight, ele sur fac tannel »non ionic oy de '? de aprtsK i aclamen t *» * 10% until apr ox imadamente 1! "J0% for 1 μeso of water pat fot-mar1 a μr imera me.-c the μr * v? (I); (b) mix lar se »μaradanu > ? d, do. the 0] 1% ha--, the aμrox i raised 10% μor1 weight cié the < omμn-, i r i e'in, of requested polymer based on s r a, the ujenie μol ín? e- »r u o axis I i u. nte lor-mador cié- * Indr-csge- *! c on water μ n i form-n uníμr eme-i. * c the lar-a cié. »hi clro l T T; and (c) read the pr e »me» t the T and the μr me »'. the IT; e * n ti nde * said < umμo, u i óu c »-, c letr and l? e- * n» an eye-catching feature that you can not miss out on < 1.0? Or i. nl? μo? -, in a lm osture of » 0 METHOD OF USE The compensation of the present invention may be used by means of a topical application to the skin, such as the spreading of the hand, of a art íc ulo, or por io ci r-leisure. 5 In general, they will join him. μiel tle, from apr? x i. mt- te 0.05 g ttasta approximately * H * g per centimeter of the skin, pref- erably * scle apr o 'umente- »0.05 tj ttasta approx imadamen le- * 7 g per square meter, C EXAMPLES TO C onl iuuac uní se μr oμer r lorian < - »ep I os the present and future n ew l l l l l o o o o o r t t) e-> e m e m e l if the specific modalities of the same, but it is not intended to necessarily limit the i nvenc ition a du bas modalities. The scope of the present document and the definition of the future, claim the following: I nq red i, in te (% weight) 1_ 7 7 4 Water 75. R7 97.10 90. OR 90.03 Age »nte» Pol imer or Re »I i f u -mi e > Hydrogel Formation * 0.4 0"4 O 0. 5 0.50 83 icein na 1, oo. oo 7.00 Ctspolymer PFR / PP0-17 to 7.00 7, "OO 3.00 Perfume 0.5? 0.50 0.75 0.7 Ficcssanato Copol mi de Di mtie oua = * 1"7 ^ 1.75 7.00 2.00 PPG-2-Ceteareto-9 * 1.75 1.75 1.50 1.50 F.DTA Disóciie.a 0.07 0.07 0.07 0.07 Hi danto ina DMDM (y) Bu ti Icarhamato de yocloμr -oμ i ni 1 on 0.70 O "70 0.70 0.70 1 Sanwet IM-1000 (Hoerhst Ce. »Anese / F i ne * Chomu als) to UC0N 75-H-45C) (Union Carbide) to FANCCRRIl I TM-1-1 (Fanning Torp ,,)" • EMUL6IN ( Hent-el Cor-f) - Errery ßroup) »Glydant Plus (lon, Tin or-μora ted) The formula tone - »*, of the previous em elo se * e > He now rum in the following way. Seventy-eight percent of the total water required for the co-location was added to a mixing mixer equipped with a rotor-stator home, and the agent was added to the shaft. - »] if?« Before- »hydragel-mixer-mixing at a speed of» 95o? Ions per minute (r-pm) in a range of 7 gr- a./mi nu increase ") see it? Mixed ulati to 74,000 > μni > I'm not even minutes. Re formed a hydroge! clear (P reme re l A). Fw a stippled r-e »t equipped with an agitator-of li or ^ blades, - > and they added from 10 to 1% of the total water available. l a. - ». l» the »ornen, • (') to a v ality of 500 rpm and the FDTA di ódit and the Rly ant Plus ™ and the μref > ar-ac i r ') i? will »me, r? until they left. F.iitont s were added the urine and the first one PFB / ÍPRPR to 17% t out of the metric in a "50 ° r-μm" until the The solution will be c lat-a (Pre erc la r '<). In the case of a separate safety device fitted with an agitator, it will be possible to remove the scent, and the US will hear it conveniently. ona and they ran at a speed of ho? rpnt has got a me / c the ttcsmocjét? e- »» »ugg-og (') the PPR-7-tterteto-9 and" continued I1"» the ezc a 500 pμm ha *, which obtained a me- the homog- »ne» the remaining amount of the water wanted was * added in the ame- »nle-» (in approximately 1 grams / null ) mixing (Pteme.-n the C).

Premix the B - > He added ^ Preme ^ cla A in a range of »about 1 gram to one of the three agitators of the» three "(» Blades, at a glance »loci idaci 50C) rpitt. Fnlonc e» s slowly added the Freme / cla C (at approximately 1 gram / minute) to the mixture of the Preme t la *. A and F-agg ng> on the three-bladed roller, at a speed of 50 ° rμ "l μer fumes ade * c nados? Nclttye * ??, by * ejecrtplcs, that! css used in the pro cesses for the care of * the foot »! Listen to Rpi ce ™ (Proi ter * &Change ») and read it. The final product is I? e omμos U I ("t t t t t t clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara clara.

Claims (1)

1. CLAIMS 1. topical, thick, thick co-positivity, perfume for the eye, the name of the person who will use it in the «* > - »| 0.1% ha -, I approve m <" i am «* nle 10%, by weight, e an age. * Le- > μol impercept or axis! i f] t to formachlor de-hidt-ogel, c lc ulated on a base? dry weight tle »] age» nte > pol tméru or gel i f je nte; (b) Approximately, »0.05% ha-, Approximately« 5% by weight »per» smoke »> ol ublt »in water; (c) from »apro, '1 fnadamen * 0.1% up to approximately 1% for * pc» so, ele »a, n (-far laute-» no? óno.o¡¡ and (d) from »Approximately« 5% is approximately »99.75%, by weight, of water, 5 e -» n where the om e sic ion e- * sc 1 It has a brightness in a temperature of 75 ° C of »μor I océnos 4,000 (the tμoi se- ■ 7. I om om omposic i c'nt to e 'le niellado of» such skin and how it is described in the Statement of Action 1, which is explained in addition to the fact that »the current policy is to protect the hydrologer A "crosslinked" or "cross-linked" sample contains monomers of unsaturated carboxylic acids onoe, or anhydrides, and anhydrides of the same type. It is described in detail in the Claim 7, which is further accrued because it says: "agent," "politician," or "translator". - tie ti i dr-csg «.-» l e »» s sele »e tonacJo of the group < c > ns tsten le de »μol ero de» cido pol i ac r-i 1 i c o, pol em ulo μol une - »-! a! r I l ira, copo! i p ers of ac cicio pol i ae i i i > o /? c telo pol urtet -te ri 1 i < or, p l i prer s anhydride derivatives and, < ? l »s fie" < > > > ri l it es / c gone melat ri'l iro y me t: 1 s ele my os sene > s 4. lac ocnpos ic ion for r- »The care of the skin and the skin will be seen in the skin, and it will be injected with the skin, because it is a polyacid agent. imeric axis- *! ifu anl c »foi ntatlot dt * hitlrocje! no I? e»? it- »a lower fabric * to approximately * 1B0 * f," 5"lt omμo u u'ni μ -tiae |» u ? lacle * of »the piol l <? lyc as st» descibe »in the F? ei vindu t, i? n 1, t ti n I er a tio n furthermore |» orque iettt) agent pol erierie ge »! If you anl c» formed) - from »Ipdr ogel no í i e-> g a Tg previous to -, des, omposi on at a temperature of» changing mind 7ooß C or mayfir b. component for the > and the first one, and the one described in the second window, can be read in more » Please note that the number of items in the 17 tINT or less. * 7. The co-position for the skinning of such a skin is described in the Claim A, also because it is a leprate and because it is a *, lurhide * / tic »aμr ox unaclaenf-» n le 15 tlMT or less. R. La cuenposi < ion μara < »1 T utelado of:» the skin such and c. It is described in Petvind 1, and also because it is said to be non-linear, the only product of the e-c &c. On the other hand, I have the option to opt for the use of the alcohol, the alcohol, the alcohol, the alcohol, the alcohol, etc. else * the same. 9. lc ompos ic ton for the t and n the skin and as it appears in the R «»? vi ndu ae ton R, c -trac - »r? _: ada adema - »By which the proportion of che bo t ool iol ti» »the uret u ona di dif lio ether of» alc hol allo loo o pulo e »to, la la» cié »de chiro -c i nly- »Ol; 1.0 up to approximately 0, 1, or 10. lat omμosic ?????????????????????????? ón 9, <arac also stressed because the proportion e ti o ho i oμe i io io in I »on to you 11 IO >» 'l? - »r tic» alc ohol alkyl μt -oμo;?! -nlf) e * to? laclo e »« d Approximately 0.5 Ü l .O to *. a |) i-t); tmatla eute 1.5 i 1, 0. 11. lc m ic t m ol ol ol ol ol ol c c c c c c describe describe describe describe describe 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11. 11.. - »of * approx one way < -j] 0.7% up to approximately- * e »l 5% de * tiu ho agent μol iménco ge! I ficante formador de »» hielroge], from »-df-» aμr-on unadanen te * e- * o.05% up to about 3% said μerfum * », and tic -» -. from »ap ox i madamente V the .1% up to approx. 1% of the said surfactant no i? N. 17. lc omμosjt ton μ-ir »» lc útela »what is pi ltlyc as it is descried in la Reí vi nd u acue 10, * arac te» p / ac aa s because »said c omposi on s »-» from «pr-ox uñadamente- * 0.7% up to ('about one-year» e] 5% dr * »h > luí agent μol unér'ic og« "* li ficante hydrogel-forming,»! » -> - »-» ox ox ately 0.05% ha *, approxi- mately * c- »7% of the perfume, and from» approximately 0.1% up to api / 1 maelafieo you 10% of the south face "oi? ni ee 5 13. the co pessie uni for the skin care as described in the Re d i I n d i I 1, In addition, because said composition 11, it has "a value" of a minimum of 7.0 (1) or approximately. , ("), 0 0 c on!? Nisi in a l? - * rrt | ter * tur a ci 75 ° C. 14. the tomposit i c'ni for the care of the skin as it is in Re ivi nd u ae u'nt 1 ', c ar e e / acia acie ás because said c ompos u? one - »*, > or μr e-ndon of .tic »a | > ? t) send me the O3% up to the last minute ** e »l 9% μoi μosp de dicht) atjentt» pol i épc or gel and fie ante forador de »h? r t) ge »l, 15. I a i oos i c uni p it. moistened with 1 i such skin and > This is described in the Pe? v? ndu ac u'ni 1, < ar-ac is also added because it includes a skin-to-skin caregiver, an agent, or resc-anle, an agent, or an e-n-t-ion, on renovating agent ci »the skin, or a combinac u'in de l -, mi, mor». 16. The procedure for skin care as set out in Claim 15 is also ruled because said agent is smeared! of the "r" s skin selected from the group consisting of glucose polyethylene glycol, polyethylene glycol polyethylene glycol esters and mono-, rl i - and Ir * ig] i cér -i two, polyether glycol ethers i no cié di di dr io 1 year! it is ele »C4 to C10, i r te» cjliccsl pol i pr p 11 e »n? / g 1 u o I lol i e 111 enio ele- * ointments and c o t) i rt c i ons» 11 > s i * .m? ts. EXCERPT FROM THE INVENTION Be »propose a clear, watery, thick, watery odors containing pe-r-fume-», I -i *. . i H 1 is e omμrende * n; (a) a watery hydroxide, roa! < am \) e-nde »do, or aμi-o, i a. lament »0.1% up to about 1 or% per-volume, of an agent μol unépco gel? f icant gel formaclor, c onc ulated above the weight of the agent pol ten ruo gel if u ule, et otj (h) ile- de apr-ox i madmeute 0.1% has tied approximately 1 % by weight, of a non-ionic, non-ionic; (c) from about 0.05% to about 15% by weight of insoluble water in water; and (d) from about 50% up to 100% by weight of water, as well as with a viscosity at a temperature of 50%. TT ^ "C tle μot at least approximately 4,000 cent ipoi is an e-tient, uf? Cient of said non-ionic sur-fac tant pair! μroμorc unt-it du ho μc- »? I smoke or for a sun, I was 1 lacla, μor what »du ba. ompo te tón is clear.