Label: CLEAR EXFOLIATING SOLUTION PAULAS CHOICE- salicylic acid cream
- NDC Code(s): 56152-5002-1, 56152-5002-2
- Packager: Cosmetic Enterprises Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 4, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
DirectionsAfter cleansing with Paula's Choice Clear Pore Normalizing Cleanser
- Cover the entire affected area with a thin layer one to three times daily
- Because excessive drying out of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
- If bothersome dryness or peeling occurs, reduce application to once a day or every other day
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INACTIVE INGREDIENT
Water (Aqua), Dipropylene Glycol, Pentylene Glycol, Polysorbate 20, Butylene Glycol, Glycerin, Sodium Hyaluronate, Dipotassium Glycrrhizate, Allantoin, Panthenol, PEG/PPG-17/6 Copolymer, Methyl Gluceth-20, Glycereth-26, Bis-PEG-18 Methyl Ether Dimethyl Silane, Sodium Hydroxide, Tetrasodium EDTA, Sodium Metabisulfite
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INGREDIENTS AND APPEARANCE
CLEAR EXFOLIATING SOLUTION PAULAS CHOICE
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:56152-5002 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 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIPROPYLENE GLYCOL (UNII: E107L85C40) PENTYLENE GLYCOL (UNII: 50C1307PZG) POLYSORBATE 20 (UNII: 7T1F30V5YH) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERIN (UNII: PDC6A3C0OX) HYALURONATE SODIUM (UNII: YSE9PPT4TH) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) ALLANTOIN (UNII: 344S277G0Z) PANTHENOL (UNII: WV9CM0O67Z) PEG/PPG-17/6 COPOLYMER (UNII: P5QZM4T259) METHYL GLUCETH-20 (UNII: J3QD0LD11P) GLYCERETH-26 (UNII: NNE56F2N14) BIS-PEG-18 METHYL ETHER DIMETHYL SILANE (UNII: OEB4R3WW9C) SODIUM HYDROXIDE (UNII: 55X04QC32I) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM METABISULFITE (UNII: 4VON5FNS3C) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:56152-5002-1 118 mL in 1 TUBE; Type 0: Not a Combination Product 08/09/2016 2 NDC:56152-5002-2 15 mL in 1 TUBE; Type 0: Not a Combination Product 08/09/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 08/09/2016 Labeler - Cosmetic Enterprises Ltd (017701475)