WO1999009936A1 - Method for treating chapped lips - Google Patents

Abstract

A method for preventing, retarding, arresting, or reversing the effects of chafed, chapped, cracked, or windburned lips comprising applying to the lips a pigmented lipstick composition comprising, by weight of the total composition: 0.01-30 % skin protectant selected from the group consisting of allantoin, cocoa butter, dimethicone, glycerin, petrolatum, shark liver oil, and mixtures thereof, 1-25 % pigment, 5-80 % of an oil selected from the group consisting of nonvolatile oil, volatile oil, and mixtures thereof, and 3-40 % of a wax having a melting point of 30 to 135 °C.

Description

METHOD FOR TREATING CHAPPED LIPS

This application is a continuation-in-part of U.S. Patent Application Serial No.

918,134. filed August 27, 1997, which is hereby incorporated by reference in its entirety.

Technical Field

The invention is in the field of pigmented cosmetic stick compositions for applying to

lips to treat chapped, chafed, or windburned lips.

Background of the Invention Chapped, chafed, or windburned lips are a problem for many women, particularly

during the cold months of the year. Chapping is a result of a lack of moisture in surface skin which affects adhesion of surface cells to the skin surface. Thus, chapped skin often appears

white and scaly due to detached surface cells.

Chapstick and other lip balms are well known treatments for such conditions.

However, lip balms are generally very waxy, unpigmented or minimally pigmented sticks that

do not provide any color to the lips. Thus, women who suffer from chapped lips who also wish to wear traditional lipstick, often will apply chapstick either before or after lipstick.

This two step process could obviously be made more convenient by formulating lipsticks

which, in addition to providing color to the lips, also prevent, retard, or arrest chapping.

Generally typical pigmented lipsticks, particularly the new transfer resistant lipsticks, do not

provide much protection against chapping. With respect to transfer resistant lipsticks, the

high concentration of volatiles quickly flashes off after application to the lips, leaving a film

which is considered by some to be somewhat dry.

It is an object of the invention to provide a full color lipstick which prevents, retards, arrests, and ameliorates the effects of chapped lips. It is a further object of the invention to provide a full color lipstick with an

appreciable concentration of volatiles, that prevents, retards, arrests, and ameliorates the

effects of chapped lips.

It is a further object of the invention to provide a full color lipstick containing

sunscreen which prevents, retards, arrests, and ameliorates the effects of chapped lips.

Summary of the Invention

The invention comprises a method for preventing, retarding, arresting, or ameliorating

the effects of chapped lips comprising applying to the lips a pigmented lipstick composition

comprising, by weight of the total composition: 0.1-30% skin protectant selected from the group consisting of allantoin. cocoa butter,

dimethicone, glycerin, petrolatum, shark liver oil. and mixtures thereof,

1-25% pigment.

5-85% of an oil selected from the group consisting of nonvolatile oil, volatile oil, and

mixtures thereof, and 3-40% of a wax having a melting point of 30 to 135° C.

Detailed Description

The term "chap" or "chapping" with respect to lips means chafed, chapped, cracked,

or windburned lips. The lipstick compositions used in the method of the invention are "full

color lipsticks", which means that they are applied to the lips as a primary lip colorant; as

opposed to a non-colored or very minimally colored sticks which do not provide any

perceivable color.

The compositions used in the method of the invention comprise 0.1-30%, preferably

0.2-25%, more preferably 0.5-20% of a skin protectant selected from the group consisting of

allantoin, cocoa butter, dimethicone, glycerin, petrolatum, shark liver oil, white petrolatum. and mixtures thereof. Preferably the skin protectant used in the method of the invention is dimethicone having a viscosity of 5 to 1,000.000 centipoise at 25° C, more preferably a

viscosity of 20 to 600,000 centipoise at 25° C.

The compositions used in the method of the invention contain 1-25%, preferably 1.5-

20%, more preferably 2-15% by weight of the total composition of pigment. Suitable

pigments include various organic and inorganic pigments. The organic pigments are

generally various aromatic types including azo. indigoid, triphenylmethane, anthraquinone, and xanthine dyes which are designated as D&C and FD&C blues, browns, greens, oranges,

reds, yellows, etc. Organic pigments generally consist of insoluble metallic salts of certified

color additives, referred to as the Lakes. Inorganic pigments include iron oxides, ultramarines, chromium, chromium hydroxide colors, and mixtures thereof.

The compositions used in the method of the invention contain 5-85%. preferably 10-

80%). more preferably 20-75% by weight of the total composition of an oil selected from the

group consisting of nonvolatile oil. volatile oil. and mixtures thereof.

With respect to the volatile oils, the term "volatile" means that the oil or solvent has a vapor pressure of at least 2 mm. of mercury at 20° C. The viscosity of the volatile solvent is

preferably 0.5 to 5 centipoise at 25° C. Such volatile solvents include volatile low viscosity

silicone fluids such as cyclic silicones having the formula:

wherein n = 3-7. Volatile linear polydimethylsiloxanes are also suitable and generally have from about 2 to 9 silicon atoms and are of the formula:

(CH₃)Si--O--[-Si-(CH₃)₂-O-]_n--Si(CH₃)₃

wherein n = 0-7. These silicones are available from various sources including Dow Corning

Corporation and General Electric. Dow Corning silicones are sold under the tradenames Dow

Corning 244. 245. 344, 345, and 200 fluids. These fluids comprise

octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, hexamethyldisiloxane, or mixtures thereof.

Also suitable as the volatile solvent component are straight or branched chain paraffinic hydrocarbons having 5-20 carbon atoms, more preferably 10-16 carbon atoms.

Suitable hydrocarbons are pentane. hexane, heptane, decane, dodecane, tetradecane.

tridecane. and C₈.₂₀ isoparaffins as disclosed in U.S. patent nos. 3,439.088 and 3,818.105, both of which are hereby incorporated by reference. Preferred volatile paraffinic hydrocarbons have a molecular weight of 70 to 190, more preferably 160-180, and a boiling

point range of 30 to 320° C, preferably 60 to 260° C. and a viscosity of less than 20

centipoise at 25° C. Such paraffinic hydrocarbons are available from EXXON under the ISOPAR trademark as ISOPAR A. B, C. D, E. G. H. K. L. and M. Similar paraffinic

hydrocarbons are also available from Shell Oil under the Shellsol trademark, in particular

Shellsol 71; and from Phillips Petroleum under the tradename Soltrol 100. 130, and 220. In

addition these paraffinic hydrocarbons may be purchased from Permethyl Corporation under

the tradename Permethyl 99A or Permethyl R.

The volatile solvent may be a mixture of volatile silicone and paraffinic hydrocarbons,

and if so, a ratio of 1 :20 to 20:1 respectively is suggested. With respect to the nonvolatile oil, the term "nonvolatile" means that the oil has a vapor pressure of less than about 2 mm. of mercury at 20° C. The nonvolatile oil generally

has a viscosity of greater than 10 centipoise at 25° C, and may range in viscosity up to

1,000,000 centipoise at 25° C, preferably 100 to 600,000 centipoise at 25° C. Preferably the

oil is a liquid to semi-solid at room temperature. Particularly preferred as the nonvolatile oil

component is a C₁₂.₂₂ fatty ester of citric acid. Preferably the fatty ester of citric acid is formed by the reaction of a C₁₂.₂₂ fatty alcohol with citric acid. One, two, or three carboxylic acid groups of the citric acid may be esterified. The fatty acid ester of citric acid generally

exhibits the following generic formula:

CH₂COOR,

OH — C-COOR₂

CH₂COOR₃

wherein R,. R₂. and R₃ are each independently H. or a C,₂.₂₂, preferably a C₁₆.₂₂ alkyl, more

preferably a C,₈.₂₂ alkyl. with the proviso that R,, R₂. and R₃ cannot all be hydrogen at the

same time. Preferably, R,. R₂. and R₃ are each a C₁₆.₂₂ alkyl, preferably isostearyl and the compound is triisostearyl citrate.

Other nonvolatile oils that may be used include esters of the formula RCO-OR' wherein

R and R' are each independently a C,_₂₅. preferably a C₄.₂₀ straight or branched chain alkyl, alkenyl

or alkoxycarbonylalkyl or alkylcarbonyloxyalkyl. Examples of such esters include isotridecyl

isononanoate, PEG-4 diheptanoate. isostearyl neopentanoate, tridecyl neopentanoate. cetyl

octanoate. cetyl palmitate. cetyl ricinoleate. cetyl stearate. cetyl myristate. coco- dicaprylate/caprate. decyl isostearate. isodecyl oleate. isodecyl neopentanoate, isohexyl neopentanoate, octyl palmitate, dioctyl malate, tridecyl octanoate, myristyl myristate, octododecanol, and fatty alcohols such as oleyl alcohol, isocetyl alcohol, and the like.

The oil may also comprise naturally occuring glyceryl esters of fatty acids, or

triglycerides. Both vegetable and animal sources may be used. Examples of such oils include

castor oil, lanolin oil, triisocetyl citrate, C₁₀_₁₈ triglycerides, caprylic/capric/triglycerides. coconut

oil, corn oil, cottonseed oil. linseed oil, mink oil, olive oil, palm oil, illipe butter, rapeseed oil,

soybean oil. sunflower seed oil, walnut oil, and the like.

Also suitable as the oil are synthetic or semi-synthetic glyceryl esters, e.g. fatty acid

mono-, di-, and triglycerides which are natural fats or oils that have been modified, for example. acetylated castor oil, glyceryl stearate. glyceryl dioleate, glyceryl distearate. glyceryl trioctanoate.

glyceryl distearate, glyceryl linoleate, glyceryl myristate. glyceryl isostearate, PEG castor oils.

PEG glyceryl oleates. PEG glyceryl stearates, PEG glyceryl tallowates. and so on.

Also suitable as the oil are nonvolatile hydrocarbons such as isoparaffins, hydrogenated polyisobutene. mineral oil. squalene, petrolatum, and so on. Straight or branched chain fatty alcohols having the formula R-OH. wherein R is a straight

or branched chain saturated or unsaturated alkyl having 6-30 carbon atoms, are also suitable oils.

Such fatty alcohols include cetyl alcohol, stearyl alcohol, cetearyl alcohol, and the like.

Also suitable as the oil are various lanolin derivatives such as acetylated lanolin,

acetylated lanolin alcohol, and so on.

Also suitable as the nonvolatile oil are various fluorinated oils such as fluorinated

silicones. fluorinated esters, or perfluropolyethers. Particularly suitable are fluorosilicones such as

trirnethylsilyl endcapped fluorosilicone oil, polytrifluoropropylmethylsiloxanes, and similar

silicones such as those disclosed in U.S. patent no. 5,118.496 which is hereby incorporated by

reference. Perfluoropolyethers like those disclosed in U.S. patent nos. 5,183,589.4.803.067. 5,183,588 all of which are hereby incorporated by reference, which are commercially available from Montefluos under the trademark Fomblin, are also suitable shine enhancers.

Guerbet esters are also suitable oils. The term "guerbet ester" means an ester which is

formed by the reaction of a guerbet alcohol having the general formula: R'-CH~CH₂OH

R²

with a carboxylic acid having the general formula:

R³COOH, or

HOOC-R³-COOH

wherein R¹ and R² are each independently a C₄.₂₀ alkyl and R³ is a substituted or unsubstituted

fatty radical such as a C,.₅₀ straight or branched chain saturated or unsaturated alkyl or alkylene. or phenyl. wherein the substituents are halogen, hydroxyl, carboxyl. and alkylcarbonylhydroxy.

Particularly preferred is a carboxylic acid wherein the R group is such to provide an ingredient

known as meadowfoam seed oil. Preferably, the guerbet ester is a fluoro-guerbet ester which is

formed by the reaction of a guerbet alcohol and carboxylic acid (as defined above), and a

fluoroalcohol having the following general formula:

CF₃~(CF₂)_n-CH₂-CH₂-OH

wherein n is from 3 to 40. Examples of suitable fluoro guerbet esters are set forth in U.S. patent no. 5,488,121which is hereby incorporated by reference. Suitable fluoro-guerbet esters are also set forth in U.S. patent no.

5.312.968 which is hereby incorporated by reference. Most preferred is a guerbet ester having the

tentative CTFA name fluoro-octyldodecyl meadowfoamate. This ester is sold by Siltech, Norcross

Georgia as Developmental Ester L61125 A, under the tradename Silube GME-F.

Preferably, the compositions used in the method of the invention comprise:

5-30% of a volatile oil. preferably cyclomethicone,

25-80% of a nonvolatile oil. preferably a C₎₆_₂₂ fatty ester of citric acid.

The lipstick compositions used in the method of the invention may contain 3-40%, preferably 5-35%, more preferably 10-30%) by weight of the total composition of a wax

having a melting point of 30-135° C., and generally includes animal waxes, plant waxes, mineral waxes, silicone waxes, synthetic waxes, and petroleum waxes.

Examples of waxes that can be used include bayberry, beeswax, candelilla, camauba,

ceresin, cetyl esters, hydrogenated jojoba oil. hydrogenated jojoba wax, hydrogenated microcrystalline wax, hydrogenated rice bran wax, japan wax. jojoba butter, jojoba esters,

jojoba wax. lanolin wax. microcrystalline wax. mink wax, montan acid wax. montan wax.

ouricury wax. ozokerite, paraffin. PEG-6 beeswax. PEG-8 beeswax, rice bran wax, shellac

wax, spent grain wax. sulfurized jojoba oil. synthetic beeswax, synthetic candelilla wax, synthetic carnauba wax, synthetic japan wax, synthetic jojoba oil. synthetic wax. stearoxy

dimethicone, dimethicone behenate. stearyl dimethicone, and the like, as well synthetic

homo- and copolymer waxes from the ethylene series.

The waxes may also be fluorinated waxes, either alone or in addition to the above-

mentioned natural or synthetic waxes, such as fluorinated dimethicone copolyols disclosed in U.S.

Patent No. 5,446,114, which is hereby incorporated by reference, having the general formula:

wherein: p is an integer ranging from 1 to 2,000;

Me is methyl;

R' is -<CH₂)-O-(EO)_a-{PO)_b-(EO)_c-H: R is -(CH₂MCF₂)_S-(CF₃); s is an integer ranging from 1 to 13:

a. b. and c are each independently integers ranging from 0 to 20:

EO is -(CH₂CH₂- OW and PO is -<CH₂CH(CH₃)- O-.

An example of such a fluorinated wax is dimethiconol fluoroalcohol dilinoleic acid, which

is sold by Siltech. Inc.. under the tradename Silwax F. Preferred waxes are ethylene homopolymers or ethylene copolymers. The molecular

weight of the ethylene homopolymer and/or copolymers used as the wax component may

vary, so long as the melting point of the homo- or copolymer either alone or in combination is

not greater than 135° C. Generally polyethylene waxes having a melting point range of 30 to

135° C. will have a molecular weight ranging from about 100 and 2,000. Preferably the

ethylene copolymers are comprised of ethylene monomer units in either repetitive or randon

sequence, in combination with monomer units of the following formula:

CH₂=CH-R,

wherein R, is a C,.₃₀ straight or branched chain saturated or unsaturated alkyl. aryl. or aralkyl,

preferably a C_M0 straight or branched chain alkyl. Examples of ethylene homo- and copolymers which may be used in the invention are set forth in U.S. Patent No. 5,556,613,

which is hereby incorporated by reference.

Preferably the lipsticks used in the method of the invention contain 0.1-20%,

preferably 0.5-15%), more preferably 1-10% by weight of the total composition of sunscreen.

The term "sunscreen" is defined as an ingredient that absorbs at least 85% of the light in the

UV range at wavelengths from 290 to 320 nanometers, but transmits UV light at wavelengths

longer than 320 nanometers. Examples of such ingredients include PABA, cinoxide, DEA-

methoxycinnamate, digalloyl trioleate, Benzophenone-8, ethyl dihydroxypropyl PABA, Octocrylene. octyl methoxycinnamate. octyl salicylate, glyceryl PABA. homosalate. menthyl

anthranilate. benzophenone-3, padimate A, padimate O, phenylbenimidazole sulfonic acid. benzophenone-4. and mixtures of such compounds. Particularly preferred is octyl

methoxycinnamate.

Particularly preferred lipsticks for use in the method of the invention comprise, by

weight of the total composition: 5-30%) cyclomethicone.

0.5-20%) dimethicone,

10-30% of a wax having a melting point of 35 to 120° C.

2-15% pigment, and

25-80% of a nonvolatile oil.

The lipsticks may be applied one. two, or more times a day as needed, in lieu of

chapstick or lip balm if desired. Use of these lipsticks on a regular basis will reduce,

ameliorate, and even prevent chapping of the lips. It is recommended that the lipstick be used

for at least one to five days to ameliorate the effects of chapping. The invention will be further described in connection with the following examples which are set forth for the purpose of illustration only.

EXAMPLE 1

Lipstick compositions were made according to the following formula:

Group 1 Ingredients

Synthetic wax 7.30 7.30 7.30

Bis-diglyceryl polyacyladipate-2 2.00 2.00 2.00 Triisostearyl citrate 40.44 40.44 40.55

Octyl methoxycinnamate 7.00 7.00 7.00

Isostearyl alcohol 1.00 1.00 1.00

Vitamin E acetate 0.10 0.10 0.10

Aloe extract 0.10 0.10 0.10 Retinyl palmitate 0.10 0.10 0.10

Ascorbyl palmitate 0.10 0.10

Methyl paraben 0.30 0.30 0.30

Propyl paraben 0.10 0.10 0.10

Dimethicone 1.20 1.20 1.20 Quaternium- 18 hectorite/triisostearyl citrate 1.75 1.75 1.75 (20:80)

Group 2 Ingredients

Titanium dioxide/trioctyldodecyl citrate 10.00 4.00 8.00 (50:50) D&C Red 7 Ca Lake/trioctyldodecyl citrate 1.20 3.30 0.80

(50:50) FD&C Yellow 5 Al. Lake/trioctyldodecyl citrate 1.10 2.80 1.60 (50:50)

Iron oxide/trioctyldodecyl citrate (60:40) 2.00 1.75 3.33 Iron oxide/trioctyldodecyl citrate (60:40) 0.30 1.95 1.33

Group 3 Ingredients

Cyclomethicone 8.00 18.00 18.00 Trioctyldodecyl citrate 2.93 3.47 2.94 Mica 2.47 2.73 2.00

Collagen amino acids 0.01 0.01 Menthol 0.50 0.50 0.50 The Group 1 Ingredients were combined and heated to 90° C. with mixing. The Group 2 Ingredients were then added and mixed thoroughly until the batch was uniform. The

Group 3 Ingredients were added. The composition was poured into molds and allowed to

cool.

EXAMPLE 2

The lipstick compositions of Example 1 were consumer tested with 18 subjects who

had normal to dry or dry lips at the beginning of the study. The 18 subjects were instructed

not to wear any lip products for six days in order to promote dryness or normalization of the

lips in order to simulate chapping. On day 7, the subjects chose a lipstick from the three available shades. Mauve, Wine, and Nudity, which were 1, 2, and 3 respectively, from Example 1. Subjects were asked to apply the test lipstick a minimum of two times per day

for the next five days. On day 12 subjects were asked to apply the lipstick and rate wear at 2,

4, and 6 hours. After 6 hours of wear on day 12, subjects removed the lipstick and were

asked to answer several questions. The following results were obtained: INITIAL APPLICATION % Subjects Who Agreed

Lips feel conditioned 89

Soothes lips 100

Lips feel moisturized 94

2-HOUR WEAR % Subjects Who Agreed

Lips feel moisturized 83

Helps condition lips 83

Prevents dryness 94 Helps improve and maintain healthier lip condition 94 4-HOUR WEAR % Subjects Who Agreed

Lips feel moisturized 78

Helps condition lips 83

Soothes lips 83

Prevents dryness 94 Helps improve and maintain healthier lip condition 94

6-HOUR WEAR % Subjects Who Agreed

Smoothes lips 67

Lips feel moisturized 67

Helps condition lips 72 Soothes lips 67

Prevents dryness 72 Helps improve and maintain a healthier lip condition 78

After the 6 hour wear test was completed, the subjects were asked to remove the

lipstick and answer the following questions: Do your lips feel... % Subjects Who Agreed

Smooth 56

Moisturized 56 Conditioned 50

Dry 22

Chapped 11

Comfortable 67

Uncomfortable 11

Only 11%) of the subjects who started the testing with normalized lips reported that their lips felt chapped at the end of the study.

EXAMPLE 3

The lipstick compositions of Example 2 were tested with 19 subjects who were

selected based upon their perception that they had dry or chapped lips. Subjects chose from the three available lipstick shades, Mauve, Wine, and Nudity; which were 1, 2, and 3 respectively, from Example 1. Subjects were asked to apply the test lipstick a minimum of

two times per day for five days. On day 12, subjects were asked to apply the lipstick and rate

wear at 2, 4, and 6 hours. After 6 hours of wear on day 12, subjects were asked to remove

their lipstick and answer several questions. The results are as follows:

INITIAL APPLICATION % Subjects Who Agreed

Lips feel conditioned 89

Soothes lips 79

Lips feel moisturized 95 2-HOUR WEAR % Subjects Who Agreed

Lips feel moisturized 100 Helps condition lips 95 Prevents dryness 95

Helps improve and maintain healthier lip condition 95

4-HOUR WEAR % Subjects Who Agreed

Lips feel moisturized 89 Helps condition lips 89 Soothes lips 84

Prevents dryness 84

Helps improve and maintain healthier lip condition 84

6-HOUR WEAR % Subjects Who Agreed

Smoothes lips 79 Lips feel moisturized 79 Helps condition lips 79 Soothes lips 79

Prevents dryness 84

Helps improve and maintain a healthier lip condition 84 After the 6 hour wear test was completed, the subjects were asked to remove the lipstick and answer the following questions:

Do your lips feel... % Subjects Who Agreed

Smooth 74 Moisturized 63

Conditioned 63

Dry 11

Chapped 0

Comfortable 68 Uncomfortable 0

None of the subjects who participated in the study based upon their perception that

they had dry lips, stated that their lips were chapped at the end of the study.

EXAMPLE 4 A total of 18 subjects, after having refrained from using any lip products for 6 days, participated in the study. Dry lips were simulated by blowing a stream of dry air over the lips

for thirty seconds. Baseline readings for lip moisture were performed on dry lips using a

Nova Dermal Phase Meter fitted with a lip probe. Baseline lower lip replicas for lip smoothing were prepared using SILFLO rubber impression material. Trained evaluator clinical evaluations for upper and lower lip dryness. roughness, flaking, cracking, and fine

lines were recorded.

After baseline readings, subjects were instructed to apply a product of their color choice selected from 1, 2, and 3, in Example 1, in an amount sufficient to cover the lips.

Subjects were asked to refrain from licking their lips prior to the 15 minute reading. After 15

minutes, the lipstick was wiped from the lips and readings were performed. Subjects were

then asked to continue using the product for 5 days and return to the laboratory for final evaluation. The following results were obtained:

% Improvement in Lip Smoothing After 5 Days of Use

Mean Standard Deviation

67.71 6.88

The above results are signficant at the 95% confidence level.

% Improvement in Moisture

Immediate After 5 Days

Mean St. Dev Mean St. Dev.

140.8 34.39 166.0 29.96

The above results are significant at the 95% confidence level. Clinical Evaluation of Lip Condition

Baseline After 5 days

Mean St. Dev. Mean St. Dev.

1.00 0.16 0.81 0.10 Dryness, upper lip

1.21 0.15 0.93 0.13 Dryness, lower lip B

1.07 0.07 0.53 0.13 Roughness, upper lip A

1.27 0.12 0.73 0.18 Roughness, lower lip A

0.20 0.11 0.20 0.11 Flaking, upper lip

0.40 0.16 0.27 0.12 Flaking, lower lip

0.53 0.17 0.20 0.11 Cracking, upper lip B

0.73 0.18 0.60 .0.16 Cracking, lower lip

1.00 0.00 1.00 0.00 Fine lines, upper lip

1.00 0.00 1.00 0.00 Fine lines, lower lip

Scoring: absent=0, mild/slight=l, moderate=2. severe=3.

A= significant improvement at 95% confidence level.

B=significant improvement at 90% confidence level.

The above results show that treatment of the lips with the lipstick compositions

mentioned herein provide improvements in lip condition.

While the invention has been described in connection with the preferred embodiment,

it is not intended to limit the scope of the invention to the particular form set forth, but, on the

contrary, it is intended to cover such alternatives, modifications, and equivalents as may be included within the spirit and scope of the invention as defined by the appended claims.

Claims

WE CLAIM:

1. A method for preventing, retarding, arresting, or reversing the effects of chafed, chapped,

cracked, or windburned lips comprising applying to the lips a pigmented lipstick composition

comprising, by weight of the total composition:

0.01-30% skin protectant selected from the group consisting of allantoin, cocoa butter,

dimethicone, glycerin, petrolatum, shark liver oil, and mixtures thereof,

1-25% pigment,

5-85% of an oil selected from the group consisting of nonvolatile oil, volatile oil, and mixtures thereof, and

3-40%) of a wax having a melting point of 30-135° C.

2. The method of claim 1 wherein the pigmented lipstick composition additionally comprises

1-10%) by weight of the total composition of sunscreen.

3. The method of claim 1 wherein the skin protectant is dimethicone.

4. The method of claim 3 wherein the oil is a mixture of a nonvolatile oil and a volatile oil.

5. The method of claim 4 wherein the lipstick composition comprises:

0.5-20%) dimethicone. 5-30%) of a volatile oil.

20-75%) of a nonvolatile oil. 1-25%) pigment, and

10-30%) of a wax having a melting point of 35 to 120° C.

6. The method of claim 5 wherein the lipstick composition additionally comprises 0.1-20%

by weight of the total composition of sunscreen.

7. The method of claim 5 wherein the lipstick is applied once per day.

8. The method of claim 5 wherein the lipstick is applied twice per day.

9. The method of claim 5 wherein the wax is an ethylene homopolymer or ethylene

copolymer.

10. The method of claim 5 wherein the volatile oil is cyclomethicone.

11. A method for preventing, retarding, arresting, or reversing the effects of chafed, chapped,

cracked, or windburned lips comprising applying to the lips a pigmented lipstick composition

comprising, by weight of the total composition: 0.5-20% dimethicone,

2-15%) pigment,

5-30%) cyclomethicone,

5-80%> of a nonvolatile oil, and

3-40%) of a wax having a melting point of 30 to 135° C.

12. The method of claim 11 wherein the nonvolatile oil comprises a C₁₆.₂₂ fatty ester of citric

acid.

13. The method of claim 11 wherein the wax is an ethylene homopolymer or ethylene

copolymer.

14. The method of claim 11 wherein the dimethicone has a viscosity of 10 to 1.000.000

centipoise at 25° C.

15. The method of claim 1 1 wherein the lipstick additionally comprises 0.1-20% by weight

of the total composition of sunscreen.