Label: CLINIQUE ACNE SOLUTIONS CLEANSING FOAM- salicylic acid liquid
- NDC Code(s): 49527-079-01, 49527-079-02
- Packager: CLINIQUE LABORATORIES LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 23, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
-
Inactive ingredients
water\aqua\eau • glycerin • butylene glycol • sodium methyl cocoyl taurate • sucrose • disodium phosphate • arginine cocoate • laminaria saccharina extract • caffeine • algae extract • cola acuminata (kola) seed extract • sea whip extract • peg/ppg-18/18 dimethicone • sodium hyaluronate • ppg-6-decyltetradeceth-30 • lactobacillus ferment • stearamidopropyl dimethylamine • acetyl glucosamine • capryloyl glycine • 10-hydroxydecanoic acid • polyquaternium-7 • phospholipids • stearic acid • sodium hydroxide • disodium edta • phenoxyethanol • chloroxylenol [iln41840]
- PRINCIPAL DISPLAY PANEL - 125 ml Bottle Label
-
INGREDIENTS AND APPEARANCE
CLINIQUE ACNE SOLUTIONS CLEANSING FOAM
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49527-079 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G) SUCROSE (UNII: C151H8M554) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) ARGININE COCOATE (UNII: 951Q8XZ62H) SACCHARINA LATISSIMA (UNII: 68CMP2MB55) CAFFEINE (UNII: 3G6A5W338E) CARRAGEENAN (UNII: 5C69YCD2YJ) COLA ACUMINATA SEED (UNII: 1F8VIW1479) PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5) DIMETHICONE (UNII: 92RU3N3Y1O) HYALURONATE SODIUM (UNII: YSE9PPT4TH) DECYLTETRADECETH-30 (UNII: 6FLU72F7LG) LIMOSILACTOBACILLUS REUTERI (UNII: 9913I24QEE) STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR) N-ACETYLGLUCOSAMINE (UNII: V956696549) CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ) 10-HYDROXYDECANOIC ACID (UNII: NP03XO416B) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) STEARIC ACID (UNII: 4ELV7Z65AP) SODIUM HYDROXIDE (UNII: 55X04QC32I) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) PHENOXYETHANOL (UNII: HIE492ZZ3T) CHLOROXYLENOL (UNII: 0F32U78V2Q) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49527-079-01 125 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/21/2020 11/23/2025 2 NDC:49527-079-02 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/02/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 07/21/2020 11/23/2025 Labeler - CLINIQUE LABORATORIES LLC (044475127) Registrant - Estee Lauder Companies Inc. (790802086) Establishment Name Address ID/FEI Business Operations PALC 078364654 label(49527-079) , pack(49527-079) Establishment Name Address ID/FEI Business Operations The Estee Lauder Inc 802599436 manufacture(49527-079) , pack(49527-079) , label(49527-079) Establishment Name Address ID/FEI Business Operations NORTHTEC LLC 943871157 label(49527-079) , pack(49527-079) Establishment Name Address ID/FEI Business Operations NORTHTEC KEYSTONE 949264774 label(49527-079) , pack(49527-079)
