Label: NEUTROGENA OIL-FREE ACNE WASH SENSITIVE SKIN FACIAL CLEANSER FRAGRANCE FREE- salicylic acid liquid
- NDC Code(s): 69968-0889-1, 69968-0889-2
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 12, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
For external use only
- Directions
- Other information
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Inactive ingredients
Water, Cocamidopropyl Hydroxysultaine, Sodium Methyl Cocoyl Taurate, Glycerin, Sodium Chloride, Sodium Hydrolyzed Potato Starch Dodecenylsuccinate, Panthenol, Chamomilla Recutita (Matricaria) Flower Extract, PEG-120 Methyl Glucose Dioleate, Cocamidopropyl PG-Dimonium Chloride Phosphate, C12-15 Alkyl Lactate, Benzalkonium Chloride, Disodium EDTA, Sodium Hydroxide
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 269 mL Bottle Label
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INGREDIENTS AND APPEARANCE
NEUTROGENA OIL-FREE ACNE WASH SENSITIVE SKIN FACIAL CLEANSER FRAGRANCE FREE
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0889 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 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) GLYCERIN (UNII: PDC6A3C0OX) SODIUM HYDROLYZED POTATO STARCH DODECENYLSUCCINATE (UNII: APY6XCX4XA) SODIUM HYDROXIDE (UNII: 55X04QC32I) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G) PANTHENOL (UNII: WV9CM0O67Z) CHAMOMILE (UNII: FGL3685T2X) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM CHLORIDE (UNII: 451W47IQ8X) PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0889-2 269 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/15/2024 2 NDC:69968-0889-1 14 mL in 1 TUBE; Type 0: Not a Combination Product 07/15/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 07/15/2024 Labeler - Kenvue Brands LLC (118772437)