Label: NEUTROGENA OIL FREE ACNE WASH- salicylic acid liquid
- NDC Code(s): 69968-0770-1, 69968-0770-2, 69968-0770-6, 69968-0770-9
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
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, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Sodium Chloride, PEG-80 Sorbitan Laurate, Citric Acid, Disodium EDTA, C12-15 Alkyl Lactate, Benzalkonium Chloride, Fragrance, Cocamidopropyl PG-Dimonium Chloride Phosphate, Glycerin, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Propylene Glycol, Sodium Hydroxide, Yellow 5, Red 40
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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
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0770 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) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM CHLORIDE (UNII: 451W47IQ8X) PEG-80 SORBITAN LAURATE (UNII: 239B50Y732) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE DISODIUM (UNII: 7FLD91C86K) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) CHAMOMILE (UNII: FGL3685T2X) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM HYDROXIDE (UNII: 55X04QC32I) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C RED NO. 40 (UNII: WZB9127XOA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0770-1 12 in 1 TRAY 07/29/2022 1 14 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:69968-0770-6 177 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/29/2022 3 NDC:69968-0770-9 269 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 07/29/2022 4 NDC:69968-0770-2 2 in 1 CARTON 07/29/2022 4 269 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 07/29/2022 Labeler - Kenvue Brands LLC (118772437)