Label: CLEARPROOF SPOT SOLUTION FOR ACNE-PRONE SKIN- salicylic acid cream
- NDC Code(s): 51531-5439-1
- Packager: Mary Kay Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated June 24, 2020
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- PURPOSE
- Directions:
- Warnings:
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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:51531-5439 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 VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) STEARETH-20 (UNII: L0Q8IK9E08) .GAMMA.-UNDECALACTONE (UNII: QB1T0AG2YL) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SUCROSE STEARATE (UNII: 274KW0O50M) BUTYL AVOCADATE (UNII: Q86RQ0D402) POLYSORBATE 20 (UNII: 7T1F30V5YH) 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:51531-5439-1 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(51531-5439)