Label: CLEARPROOF SPOT SOLUTION FOR ACNE-PRONE SKIN- salicylic acid cream
- NDC Code(s): 51531-8953-1
- Packager: Mary Kay Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated December 8, 2020
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- Official Label (Printer Friendly)
- PURPOSE
- Directions:
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Warnings:
For external use only.
Not to be used on children.
Do not apply to the eyelids, the edges of the nose and mouth, or to irritated or damaged slin.
Avoid the eye area.
For use during pregnancy, consult your doctor.
Avoid sun exposure when using this product.
In the first applications, you may experience a transient burning sensation or itchy or dry skin.
If the discomfort persists, discontinue use of the product and consult your doctor.
Keep out of the reach of children. Do not ingest
In case of accidental contact with the eyes, rinse thoroughly with water.
If irritation develops, discontinue use and consult your doctor.
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INGREDIENTS:
AQUA, ETHYLHEXYL PALMITATE, STEARYL ALCOHOL, GLYCERIN, SALICYLIC ACID, TRIETHANOLAMINE,
CYCLOPENTASILOXANE, POLYSORBATE 60, PROPYLENE GLYCOL, GLYCERYL STEARATE,
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, BUTYL AVOCADATE, ETHYLENE/ACRYLIC ACID COPOLYMER, RETINYL PALMITATE, STEARETH-20, PEG-100 STEARATE, POLYACRYLATE-13, SUCROSE DISTEARATE, CETEARYL ALCOHOL, DIMETHICONE CROSSPOLYMER, SUCROSE STEARATE, POLYISOBUTENE, ARCTIUM LAPPA
ROOT EXTRACT, CITRIC ACID, DISODIUM EDTA, TITANIUM DIOXIDE/CI 77891, METHYLDIHYDROJASMONATE, C12-14
PARETH-12, EPILOBIUM ANGUSTIFOLIUM FLOWER/ LEAF/STEM EXTRACT, POLYSORBATE 20, CYCLOHEXASILOXANE, ETHYLENE BRASSYLATE, ETHYL LINALOOL, PHENOXYETHANOL, BUTYLENE GLYCOL, ISOBUTYL METHYL
TETRAHYDROPYRANOL, METHYLENEDIOXYPHENYL METHYLPROPANAL, METHYLPARABEN, CYSTOSEIRA
AMENTACEA/CAESPITOSA/BRANCHYCARPA EXTRACT, CHLORPHENESIN, GAMMA-UNDECALACTONE, BENZOIC
ACID, CYCLAMEN ALDEHYDE, SODIUM METABISULFITE, PROPYL GALLATE, CI 19140, CI 17200, CI 42090 - Principal Display Panel - 29 g carton
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INGREDIENTS AND APPEARANCE
CLEARPROOF SPOT SOLUTION FOR ACNE-PRONE SKIN
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51531-8953 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 g Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SUCROSE STEARATE (UNII: 274KW0O50M) BUTYL AVOCADATE (UNII: Q86RQ0D402) POLYSORBATE 20 (UNII: 7T1F30V5YH) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) STEARETH-20 (UNII: L0Q8IK9E08) .GAMMA.-UNDECALACTONE (UNII: QB1T0AG2YL) GLYCERIN (UNII: PDC6A3C0OX) PEG-100 STEARATE (UNII: YD01N1999R) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD) ETHYLHEXYL PALMITATE (UNII: 2865993309) TROLAMINE (UNII: 9O3K93S3TK) POLYSORBATE 60 (UNII: CAL22UVI4M) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y) EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D) CYCLOMETHICONE 6 (UNII: XHK3U310BA) ETHYL LINALOOL (UNII: SF2JS9GF5T) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) 3-(3,4-METHYLENEDIOXYPHENYL)-2-METHYLPROPANAL (UNII: L65EG8H6PA) METHYLPARABEN (UNII: A2I8C7HI9T) CHLORPHENESIN (UNII: I670DAL4SZ) BENZOIC ACID (UNII: 8SKN0B0MIM) CYCLAMEN ALDEHYDE (UNII: 4U37UX0E1E) D&C RED NO. 33 (UNII: 9DBA0SBB0L) WATER (UNII: 059QF0KO0R) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) SUCROSE DISTEARATE (UNII: 33X4X4B90S) POLYISOBUTYLENE (2300 MW) (UNII: DSQ2V1DD1K) ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I) C12-14 PARETH-12 (UNII: M0LJS773XW) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE DISODIUM (UNII: 7FLD91C86K) 2-ISOBUTYL-4-METHYLTETRAHYDROPYRAN-4-OL (UNII: VK5ZHH2T3F) SODIUM METABISULFITE (UNII: 4VON5FNS3C) PROPYL GALLATE (UNII: 8D4SNN7V92) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51531-8953-1 1 in 1 CARTON 11/30/2017 1 29 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Export only 11/30/2017 Labeler - Mary Kay Inc. (049994452) Establishment Name Address ID/FEI Business Operations Mary Kay Inc. 103978839 manufacture(51531-8953)
