Label: CLINIQUE ACNE SOLUTIONS CLEANSING FOAM- salicylic acid liquid
- NDC Code(s): 49527-119-01, 49527-119-02
- Packager: CLINIQUE LABORATORIES LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated April 12, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
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Directions
- pump dispenser 2-3 times
- massage gently over wet skin, avoiding eye area
- rinse
- follow with Acne Solutions Clarifying Lotion
- if bothersome drying or peeling occurs, reduce usage to every other day
- because excessive drying of the skin may occur, start with one use daily, then gradually increase to twice a day if needed or as directed by a doctor
- after acne clears, continue using for preventative care
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Inactive ingredients
water\aqua\eau,glycerin,sodium methyl cocoyl taurate,butylene glycol,sucrose,disodium phosphate,salicylic acid,sodium hyaluronate,phosphatidylcholine,caffeine,cola acuminata seed extract,algae extract,laminaria saccharina extract,lactobacillus ferment,stearamidopropyl dimethylamine,acetyl glucosamine,10-hydroxydecanoic acid,arginine cocoate,peg/ppg-18/18 dimethicone,capryloyl glycine,ppg-6-decyltetradeceth-30,stearic acid,polyquaternium-7,disodium edta,phenoxyethanol,chloroxylenol,sodium benzoate <iln53446>
- PRINCIPAL DISPLAY PANEL - 125 ml Bottle Label
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INGREDIENTS AND APPEARANCE
CLINIQUE ACNE SOLUTIONS CLEANSING FOAM
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49527-119 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 15 mg in 1 mL Inactive Ingredients Ingredient Name Strength PHOSPHATIDYLCHOLINE, SOYBEAN (UNII: 1T6N4D9YV6) PORPHYRIDIUM PURPUREUM (UNII: K2P8K2558N) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) 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) COLA ACUMINATA SEED (UNII: 1F8VIW1479) HYALURONATE SODIUM (UNII: YSE9PPT4TH) 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) STEARIC ACID (UNII: 4ELV7Z65AP) 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:49527-119-01 125 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/15/2024 2 NDC:49527-119-02 1 in 1 CARTON 04/15/2024 2 50 mL in 1 BOTTLE, PUMP; 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 04/15/2024 Labeler - CLINIQUE LABORATORIES LLC (044475127) Registrant - Estee Lauder Companies Inc. (790802086) Establishment Name Address ID/FEI Business Operations The Estee Lauder Inc 802599436 manufacture(49527-119) Establishment Name Address ID/FEI Business Operations NORTHTEC KEYSTONE 949264774 label(49527-119) , pack(49527-119) Establishment Name Address ID/FEI Business Operations NORTHTEC LLC 943871157 label(49527-119) , pack(49527-119)