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
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 5, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- NOXZEMA ULTIMATE CLEAR ANIT-BLEMISH DAILY SCRUB- (Salicylic Acid) emulsion
- Drug Facts
- Active ingredient
- Purpose
- Uses
- Warnings
-
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.
-
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.
- Questions?
- Packaging
-
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 final part333D 10/01/2012 Labeler - CONOPCO Inc. d/b/a Unilever (001375088)
