Label: BLACKHEAD SOLUTIONS 7 DAY DEEP PORE CLEANSE AND SCRUB ACNE MEDICATION- salicylic acid cream
- NDC Code(s): 49527-062-01, 49527-062-02
- Packager: CLINIQUE LABORATORIES LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 25, 2024
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
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Inactive ingredients
water\aqua\eau • kaolin • glycerin • butylene glycol • magnesium aluminum silicate • glyceryl stearate • peg-100 stearate • silica • sodium lauroyl sarcosinate • allyl methacrylates crosspolymer • gentiana lutea (gentian) root extract • laminaria saccharina extract • sucrose • acetyl glucosamine • caprylyl glycol • 1,2-hexanediol • tocopheryl acetate • sodium hydroxide • xanthan gum • disodium edta • phenoxyethanol • titanium dioxide (ci 77891) • blue 1 (ci 42090) • yellow 5 (ci 19140) [iln43442]
- PRINCIPAL DISPLAY PANEL - 15 ml Bottle Carton
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INGREDIENTS AND APPEARANCE
BLACKHEAD SOLUTIONS 7 DAY DEEP PORE CLEANSE AND SCRUB ACNE MEDICATION
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49527-062 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) KAOLIN (UNII: 24H4NWX5CO) GLYCERIN (UNII: PDC6A3C0OX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) SUCROSE (UNII: C151H8M554) N-ACETYLGLUCOSAMINE (UNII: V956696549) CAPRYLYL GLYCOL (UNII: 00YIU5438U) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) SODIUM HYDROXIDE (UNII: 55X04QC32I) XANTHAN GUM (UNII: TTV12P4NEE) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) PHENOXYETHANOL (UNII: HIE492ZZ3T) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) 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:49527-062-01 1 in 1 CARTON 08/30/2018 11/30/2022 1 20 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:49527-062-02 1 in 1 CARTON 08/01/2022 2 125 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 08/30/2018 Labeler - CLINIQUE LABORATORIES LLC (044475127) Registrant - Estee Lauder Companies Inc. (790802086) Establishment Name Address ID/FEI Business Operations PALC 078364654 pack(49527-062) , label(49527-062) Establishment Name Address ID/FEI Business Operations Northtec LLC 943871157 pack(49527-062) , label(49527-062) Establishment Name Address ID/FEI Business Operations The Estee Lauder Inc 802599436 label(49527-062) , manufacture(49527-062) , pack(49527-062)