Label: ST. IVES BLEMISH AND BLACKHEAD CONTROL APRICOT SCRUB- salicylic acid emulsion
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Contains inactivated NDC Code(s)
NDC Code(s): 64942-1245-1, 64942-1245-2, 64942-1245-3, 64942-1245-4 - 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 November 5, 2013
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- Official Label (Printer Friendly)
- 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), Juglans Regia (Walnut) Shell Powder, Glycol Stearate SE, Glycerin, Sodium Lauryl Sulfoacetate, Zea Mays (Corn) Kernel Meal, Cocamidopropyl Betaine, Cetearyl Alcohol, Triethanolamine, Cetyl Alcohol, Glyceryl Stearate, PEG-100 Stearate, Prunus Armeniaca (Apricot) Fruit Extract, Cetyl Acetate, Ceteareth-20, Carbomer, Polysorbate 60, Acetylated Lanolin Alcohol, Fragrance (Parfum), PPG-2 Methyl Ether, Phenethyl Alcohol, Methylisothiazolinone, Titanium Dioxide (CI 77891).
- QUESTIONS
- 6 oz PDP
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INGREDIENTS AND APPEARANCE
ST. IVES BLEMISH AND BLACKHEAD CONTROL APRICOT SCRUB
salicylic acid emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1245 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 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) JUGLANS REGIA SHELL (UNII: PJ10MT7VKA) Glycerin (UNII: PDC6A3C0OX) SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) CORN GRAIN (UNII: C1Z9U7094Z) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) TROLAMINE (UNII: 9O3K93S3TK) CETYL ALCOHOL (UNII: 936JST6JCN) PEG-100 STEARATE (UNII: YD01N1999R) APRICOT (UNII: 269CJD5GZ9) CETYL ACETATE (UNII: 4Q43814HXS) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) POLYSORBATE 60 (UNII: CAL22UVI4M) PHENYLETHYL ALCOHOL (UNII: ML9LGA7468) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P) PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1245-1 283 g in 1 JAR 2 NDC:64942-1245-2 212 g in 1 TUBE 3 NDC:64942-1245-3 170 g in 1 TUBE 4 NDC:64942-1245-4 28 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 03/01/2012 Labeler - CONOPCO Inc. d/b/a Unilever (001375088) Establishment Name Address ID/FEI Business Operations Unilever Manufacturing (US), Inc. 021679448 manufacture(64942-1245)
