Label: ST. IVES- salicylic acid emulsion
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Contains inactivated NDC Code(s)
NDC Code(s): 12488-0500-9 - Packager: Alberto-Culver USA Inc.
- 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 February 16, 2011
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- Official Label (Printer Friendly)
- DRUG FACTS
- Active Ingredient
- Purpose
- Use
- Warnings
- Directions
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Inactive Ingredients
Water, Sodium Laureth Sulfate, Bentonite, Cocamidopropyl Betaine, Acrylates Copolymer, Epilobium Angustifolium Extract, Olea Europaea (Olive) Leaf Extract, Ascophyllum Nodosum Extract, Alteromonas Ferment Extract, Yeast Extract, Camellia Sinensis Leaf Extract, Sodium Hydroxide, Glycerin, Disodium EDTA, Polyquaternium-7, Phenethyl Alcohol, PPG-2 Methyl Ether, Methylisothiazolinone, Fragrance, Green 5, Yellow 10, Yellow 5, Red 4, Red 33, Blue 1.
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- PRINCIPAL DISPLAY PANEL - 266 mL Bottle Label
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INGREDIENTS AND APPEARANCE
ST. IVES BODY SCRUB NATURALLY CLEAR SKIN GREEN TEA
salicylic acid emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:12488-0500 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 mL in 1 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Sodium Laureth Sulfate (UNII: BPV390UAP0) Bentonite (UNII: A3N5ZCN45C) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) Sodium Hydroxide (UNII: 55X04QC32I) Glycerin (UNII: PDC6A3C0OX) Edetate Disodium (UNII: 7FLD91C86K) Phenylethyl Alcohol (UNII: ML9LGA7468) Olea Europaea Leaf (UNII: MJ95C3OH47) Ascophyllum Nodosum (UNII: 168S4EO8YJ) Methylisothiazolinone (UNII: 229D0E1QFA) D&C Green No. 5 (UNII: 8J6RDU8L9X) D&C Yellow No. 10 (UNII: 35SW5USQ3G) Yeast (UNII: 3NY3SM6B8U) Green Tea Leaf (UNII: W2ZU1RY8B0) Fd&C Yellow No. 5 (UNII: I753WB2F1M) Fd&C Red No. 4 (UNII: X3W0AM1JLX) Fd&C Blue No. 1 (UNII: H3R47K3TBD) D&C Red No. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:12488-0500-9 266 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part333D 02/14/2011 Labeler - Alberto-Culver USA Inc. (021679448) Establishment Name Address ID/FEI Business Operations Alberto-Culver USA Inc. 021679448 ANALYSIS, MANUFACTURE Establishment Name Address ID/FEI Business Operations Cosmetic Laboratories of America 617165329 ANALYSIS, MANUFACTURE