Label: ST. IVES BLEMISH AND BLACKHEAD FACIAL- salicylic acid soap
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Contains inactivated NDC Code(s)
NDC Code(s): 12488-0200-1 - 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 December 17, 2009
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- INDICATIONS & USAGE
- Warnings
- Directions
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OTHER INGREDIENTS
Water (Aqua, Eau), Sodium Laureth Sulfate, Glycerin, Cocamidopropyl Betaine, Propylene Glycol, Disodium Laureth Sulfosuccinate, Hydroxyethyl Urea, Acrylates/Aminoacrylates/C10-30 Alkyl PEG-20 Itaconate Copolymer, Jojoba Esters, DMDM Hydantoin, Fragrance (Parfum), Menthyl Lactate, Hydroxyethylcellulose, Disodium EDTA, Silica, Betaine, Sodium PCA, Butylphenyl Methylpropional, Benzyl Benzoate, Triethanolamine, Sorbitol, Amyl Cinnamal, Limonene, Iodopropynyl Butylcarbamate, Mica (CI 77019), Titanium Dioxide (CI 77891), Proline, Linalool, Yellow 5 Lake (CI 19140), Red 30 Lake (CI 73360), Geraniol, Serine, Glycine, Glutamic Acid, Alanine, Arginine, Lysine, Salix Alba (Willow) Bark Extract, Prunus Armeniaca (Apricot) Fruit Extract, Threonine, Sambucus Nigra Flower Extract, Primula Veris Extract, Helianthus Annuus (Sunflower) Extract, Chamomilla Recutita (Matricaria) Flower Extract, Niacinamide, Ascorbic Acid.
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- PRINCIPAL DISPLAY PANEL - 170g Tube
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INGREDIENTS AND APPEARANCE
ST. IVES BLEMISH AND BLACKHEAD FACIAL
salicylic acid soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:12488-0200 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) Edetate Disodium (UNII: 7FLD91C86K) Sodium Laureth Sulfate (UNII: BPV390UAP0) Glycerin (UNII: PDC6A3C0OX) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) Trolamine (UNII: 9O3K93S3TK) Primula Veris (UNII: W6LFQ57E4M) Iodopropynyl Butylcarbamate (UNII: 603P14DHEB) Betaine (UNII: 3SCV180C9W) Sodium Pyrrolidone Carboxylate (UNII: 469OTG57A2) Sorbitol (UNII: 506T60A25R) Serine (UNII: 452VLY9402) Glycine (UNII: TE7660XO1C) Glutamic Acid (UNII: 3KX376GY7L) Lysine (UNII: K3Z4F929H6) Alanine (UNII: OF5P57N2ZX) Arginine (UNII: 94ZLA3W45F) Threonine (UNII: 2ZD004190S) Proline (UNII: 9DLQ4CIU6V) Disodium Laureth Sulfosuccinate (UNII: D6DH1DTN7E) Silicon Dioxide (UNII: ETJ7Z6XBU4) Titanium Dioxide (UNII: 15FIX9V2JP) Niacinamide (UNII: 25X51I8RD4) Propylene Glycol (UNII: 6DC9Q167V3) Ascorbic Acid (UNII: PQ6CK8PD0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:12488-0200-1 192 mL in 1 BOTTLE, PUMP Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part333D 06/01/2009 Labeler - Alberto-Culver USA Inc. (021679448) Establishment Name Address ID/FEI Business Operations Alberto-Culver USA Inc. 021679448 ANALYSIS, MANUFACTURE