Label: ST. IVES BLEMISH CONTROL GREEN TEA SCRUB- salicylic acid emulsion
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Contains inactivated NDC Code(s)
NDC Code(s): 64942-1296-1, 64942-1296-2 - Packager: CONOPCO Inc. d/b/a Unilever
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 30, 2013
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
Directions Clean the skin thoroughly before applying this product.Cover the entire affected area with a thin layer and rinse thoroughly one to three times daily. 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 ingredients
Water (Aqua, Eau), Hydrated Silica, Potassium Laureth Phosphate, Glycerin, Sodium Lauroamphoacetate, Sodium Methyl 2-Sulfolaurate, Polyacrylate-1 Crosspolymer, Citric Acid, Glycereth-18 Ethylhexanoate, Disodium 2-Sulfolaurate, Kaolin, Hydrolyzed Jojoba Esters, Fragrance (Parfum), Glycereth-18, Phenethyl Alcohol, PPG-2 Methyl Ether, Olea Europaea (Olive) Leaf Extract, Camellia Sinensis Leaf Extract, Methylisothiazolinone, Yellow 5 (CI 19140), Red 4 (CI 14700), Red 33 (CI 17200), Blue 1 (CI 42090).
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ST. IVES BLEMISH CONTROL GREEN TEA SCRUB
salicylic acid emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1296 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid 0.01 g in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) HYDRATED SILICA (UNII: Y6O7T4G8P9) GLYCERIN (UNII: PDC6A3C0OX) SODIUM LAUROAMPHOACETATE (UNII: SLK428451L) SODIUM METHYL 2-SULFOLAURATE (UNII: I39GGJ23HV) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERETH-18 ETHYLHEXANOATE (UNII: IWS58C6V2Y) DISODIUM 2-SULFOLAURATE (UNII: 329M3829G2) KAOLIN (UNII: 24H4NWX5CO) HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W) GLYCERETH-18 (UNII: SA5E43C17C) PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N) PHENYLETHYL ALCOHOL (UNII: ML9LGA7468) OLEA EUROPAEA LEAF (UNII: MJ95C3OH47) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) GREEN TEA LEAF (UNII: W2ZU1RY8B0) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C RED NO. 4 (UNII: X3W0AM1JLX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1296-1 133 mL in 1 TUBE 2 NDC:64942-1296-2 29 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 06/15/2013 Labeler - CONOPCO Inc. d/b/a Unilever (001375088) Establishment Name Address ID/FEI Business Operations Alberto-Culver USA Inc. 021679448 manufacture(64942-1296)
