Label: NOXZEMA ANTIBLEMISH DAILY SCRUB- salicyclic acid soap
- NDC Code(s): 64942-1265-1
- Packager: CONOPCO Inc. d/b/a Unilever
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2024
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- Official Label (Printer Friendly)
- NOXZEMA ULTIMATE CLEAR ANIT-BLEMISH DAILY SCRUB- (Salicylic Acid) emulsion
- Drug Facts
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- Clean the skin thoroughly before applying 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.
Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
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Inactive ingredients
Water (Aqua), Hydrated Silica, Glycerin, Glyceryl Stearate SE, Cetearyl Alcohol, Sodium Lauryl Sulfoacetate, Cocamidopropyl Betaine, Cetyl Alcohol, Triethanolamine, Cetyl Acetate, PEG-100 Stearate, Glyceryl Stearate, Benzyl Alcohol, Carbomer, Fragrance (Parfum), Ceteareth-20, Polysorbate 60, Disodium EDTA, Benzoic Acid, Acetylated Lanolin Alcohol, Sorbic Acid, Eucalyptus Globulus Leaf Extract, Citronellol, Hexyl Cinnamal, Limonene, Linalool.
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INGREDIENTS AND APPEARANCE
NOXZEMA ANTIBLEMISH DAILY SCRUB
salicyclic acid soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1265 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 g in 1 g Inactive Ingredients Ingredient Name Strength EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) CETYL ALCOHOL (UNII: 936JST6JCN) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CETYL ACETATE (UNII: 4Q43814HXS) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J) BENZYL ALCOHOL (UNII: LKG8494WBH) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) BENZOIC ACID (UNII: 8SKN0B0MIM) ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P) SORBIC ACID (UNII: X045WJ989B) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) LIMONENE, (+)- (UNII: GFD7C86Q1W) LINALOOL, (+/-)- (UNII: D81QY6I88E) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) POLYSORBATE 60 (UNII: CAL22UVI4M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1265-1 141 g in 1 TUBE; Type 0: Not a Combination Product 10/01/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 10/01/2012 Labeler - CONOPCO Inc. d/b/a Unilever (001375088)
