Label: UP AND UP BLEMISH CONTROLLING APRICOT SCRUB- salicylic acid emulsion
- NDC Code(s): 11673-930-15
- Packager: TARGET CORPORATION
- 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 July 7, 2021
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Keep out of reach of children.
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Directions
• cover the entire affected area with a thin layer and rinse thoroughly one to three times daily• if bothersome dryness or peeling occurs, reduce application to once a day or every other day• 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.
- Other information
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Inactive ingredients
Water, Juglans Regia (Walnut) Shell Powder, Glyceryl Stearate SE, Propylene Glycol, Sodium Laureth Sulfate, Zea Mays (Corn) Kernel Meal, Cocamidopropyl Betaine, Cetearyl Alcohol, Triethanolamine, Cetyl Alcohol, PEG-100 Stearate, Glyceryl Stearate, Cetyl Acetate, Ceteareth-20, Polysorbate 60, Carbomer, Acetylated Lanolin Alcohol, Fragrance (Parfum), Phenethyl Alcohol, PPG-2-Methyl Ether, Limonene, Linalool, Methylisothiazolinone, Glycerin, Prunus Armeniaca (Apricot) Fruit Extract, Titanium Dioxide (CI177891).
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
UP AND UP BLEMISH CONTROLLING APRICOT SCRUB
salicylic acid emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-930 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 g Inactive Ingredients Ingredient Name Strength POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) CORN GRAIN (UNII: C1Z9U7094Z) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCERIN (UNII: PDC6A3C0OX) CETYL ALCOHOL (UNII: 936JST6JCN) GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947) ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N) APRICOT (UNII: 269CJD5GZ9) LIMONENE, (+/-)- (UNII: 9MC3I34447) WATER (UNII: 059QF0KO0R) CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208) JUGLANS REGIA SHELL (UNII: PJ10MT7VKA) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ACETATE (UNII: 4Q43814HXS) POLYSORBATE 60 (UNII: CAL22UVI4M) TROLAMINE (UNII: 9O3K93S3TK) PHENYLETHYL ALCOHOL (UNII: ML9LGA7468) LINALOOL, (+/-)- (UNII: D81QY6I88E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-930-15 170 g in 1 TUBE; Type 0: Not a Combination Product 09/25/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 09/25/2013 Labeler - TARGET CORPORATION (006961700)