Label: CLEAR ACNE BODY PAULAS CHOICE- salicylic acid spray
- NDC Code(s): 56152-5000-1
- Packager: Cosmetic Enterprises Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 19, 2023
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- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
Directions
After cleansing with Paula's Choice Clear Pore Normalizing Cleanser and exfoliating with Paula's Choice Clear Anti-Redness Exfoliating Solution.
Cover the entire affected area with a thin layer one to three times daily.
Hold container 4 to 6 inches from the skin to apply.
Do not spray directly into face. Spray on hands, then apply to face.
Because excessive drying 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
Inactive ingredientsWater (Aqua), Dipropylene Glycol, Butylene Glycol, Polysorbate 20, Pentylene Glycol, Panthenol, Sodium Hyaluronate, Dipotassium Glycyrrhizate, Glycyrrhiza Glabra (Licorice) Root Extract, Berberis Vulgaris (Barberry) Root Extract, Lauric Acid, Allantoin, Glycerin, PEG/PPG-17/6 Copolymer, Methyl Gluceth-20, Glycereth-26, Sodium Hydroxide, Sodium Metabisulfite, Disodium EDTA, Potassium Sorbate
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLEAR ACNE BODY PAULAS CHOICE
salicylic acid sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:56152-5000 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 118 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIPROPYLENE GLYCOL (UNII: E107L85C40) POLYSORBATE 20 (UNII: 7T1F30V5YH) PENTYLENE GLYCOL (UNII: 50C1307PZG) PANTHENOL (UNII: WV9CM0O67Z) HYALURONATE SODIUM (UNII: YSE9PPT4TH) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) BERBERIS VULGARIS ROOT (UNII: ITJ40JX79U) LAURIC ACID (UNII: 1160N9NU9U) ALLANTOIN (UNII: 344S277G0Z) GLYCERIN (UNII: PDC6A3C0OX) PEG/PPG-17/6 COPOLYMER (UNII: P5QZM4T259) METHYL GLUCETH-20 (UNII: J3QD0LD11P) GLYCERETH-26 (UNII: NNE56F2N14) SODIUM HYDROXIDE (UNII: 55X04QC32I) SODIUM METABISULFITE (UNII: 4VON5FNS3C) EDETATE DISODIUM (UNII: 7FLD91C86K) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:56152-5000-1 118 mL in 1 BOTTLE, SPRAY; 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)