Label: ST. IVES GREEN TEA CLEANSER- salicylic acid emulsion
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Contains inactivated NDC Code(s)
NDC Code(s): 64942-1297-1 - 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 ingredientsWater (Aqua), Sodium Laureth Sulfate, Glycerin, Cocamidopropyl Betaine, Propylene Glycol, Hydroxyethyl Urea, Disodium Laureth Sulfosuccinate, Fragrance (Parfum), Sodium Hydroxide, Menthyl Lactate, PEG-150 Distearate, Disodium EDTA, PPG-2 Methyl Ether, Phenethyl Alcohol, Methylisothiazolinone, Camellia Sinensis Leaf Extract, Olea Europaea (Olive) Leaf Extract, Green 5 (CI 61570), Yellow 5 (CI 19140), Red 33 (CI 17200), Red 4 (CI 14700), Blue 1 (CI 42090)
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INGREDIENTS AND APPEARANCE
ST. IVES GREEN TEA CLEANSER
salicylic acid emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1297 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid 0.02 g in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) GLYCERIN (UNII: PDC6A3C0OX) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR) DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) SODIUM HYDROXIDE (UNII: 55X04QC32I) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) EDETATE DISODIUM (UNII: 7FLD91C86K) PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N) PHENYLETHYL ALCOHOL (UNII: ML9LGA7468) OLEA EUROPAEA LEAF (UNII: MJ95C3OH47) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) GREEN TEA LEAF (UNII: W2ZU1RY8B0) D&C Green No. 5 (UNII: 8J6RDU8L9X) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C RED NO. 4 (UNII: X3W0AM1JLX) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1297-1 200 mL in 1 BOTTLE 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(64942-1297)