Label: NEUTROGENA OIL-FREE ACNE WASH DAILY SCRUB- salicylic acid gel
- NDC Code(s): 69968-0075-4
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Use
-
Warnings
For external use only.
- Directions
-
Other information
-
Sunburn Alert
This product contains an alpha hydroxyl acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing and limit sun exposure while using this product and for a week afterwards. Store at Room Temperature.
-
Sunburn Alert
-
Inactive ingredients
water, cetyl alcohol, PPG-15 stearyl ether, cellulose, glycerin, Polysorbate 60, steareth-21, C12-15 alkyl lactate, glycolic acid, cetyl lactate, potassium cetyl phosphate, sodium hydroxide, xanthan gum, cocamedopropyl PG-dimonium chloride phosphate, disodium EDTA, fragrance, menthol, Benzalkonium chloride, agar, BHT, sodium benzotriazolyl, butylphenone sulfonate, iron oxides, mica, yellow 5, titanium dioxide, red 30, red 40
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 124 mL Tube Label
-
INGREDIENTS AND APPEARANCE
NEUTROGENA OIL-FREE ACNE WASH DAILY SCRUB
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0075 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) CETYL ALCOHOL (UNII: 936JST6JCN) PPG-15 STEARYL ETHER (UNII: 1II18XLS1L) POWDERED CELLULOSE (UNII: SMD1X3XO9M) STEARETH-21 (UNII: 53J3F32P58) GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 60 (UNII: CAL22UVI4M) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) GLYCOLIC ACID (UNII: 0WT12SX38S) CETYL LACTATE (UNII: A7EVH2RK4O) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM HYDROXIDE (UNII: 55X04QC32I) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) EDETATE DISODIUM (UNII: 7FLD91C86K) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) AGAR, UNSPECIFIED (UNII: 89T13OHQ2B) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z) FERRIC OXIDE RED (UNII: 1K09F3G675) MICA (UNII: V8A1AW0880) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) D&C RED NO. 30 (UNII: 2S42T2808B) FD&C RED NO. 40 (UNII: WZB9127XOA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0075-4 124 mL in 1 TUBE; Type 0: Not a Combination Product 06/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 06/01/2016 Labeler - Kenvue Brands LLC (118772437)