Label: ST. IVES GREEN TEA SCRUB- salicylic acid emulsion
-
Contains inactivated NDC Code(s)
NDC Code(s): 64942-1247-1, 64942-1247-2 - 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 March 8, 2012
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
-
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 Salicylic Acid Hydrolyzed Jojoba Esters Parfum (Fragrance) Glycereth-18 Phenethyl Alcohol PPG-2 Methyl Ether Epilobium Angustifolium Extract Olea Europaea (Olive) Leaf Extract Alteromonas Ferment Extract Ascophyllum Nodosum Extract Methylisothiazolinone Yellow 5 (CI 19140) CI 14700 (Red 4) CI 17200 (Red 33) CI 42090 (Blue 1) Camellia Sinensis Leaf Extract Yeast Extract
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ST. IVES GREEN TEA SCRUB
salicylic acid emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1247 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 mL 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) ASCOPHYLLUM NODOSUM (UNII: 168S4EO8YJ) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) YEAST (UNII: 3NY3SM6B8U) 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:64942-1247-1 133 mL in 1 TUBE 2 NDC:64942-1247-2 30 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 03/08/2012 Labeler - CONOPCO Inc. d/b/a Unilever (001375088) Establishment Name Address ID/FEI Business Operations Alberto-Culver USA Inc. 021679448 manufacture