Label: NEUTROGENA RAPID CLEAR 2 IN 1 FIGHT AND FADE TONER- salicylic acid solution
- NDC Code(s): 69968-0158-8
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 11, 2024
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- Official Label (Printer Friendly)
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- Active ingredient
- Purpose
- Use
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Warnings
For external use only.
Flammable: Keep away from fire or flame.
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Directions
- Cleanse skin thoroughly before applying this product
- Cover the entire affected area with a thin layer 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.
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Other information
Sunburn Alert
This product contains an alpha hydroxy 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.
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Inactive ingredients
water, alcohol denat., butylene glycol, PPG-5-ceteth-20, C12-15 alkyl lactate, sodium citrate, fragrance, cocamidopropyl PG-dimonium chloride phosphate, PEG/PPG-20/6 dimethicone, cetyl lactate, benzalkonium chloride, sodium benzotriazolyl butylphenol sulfonate, disodium EDTA, sodium hydroxide, glycolic acid, yellow 6, red 40
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- PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label
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INGREDIENTS AND APPEARANCE
NEUTROGENA RAPID CLEAR 2 IN 1 FIGHT AND FADE TONER
salicylic acid solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0158 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) ALCOHOL (UNII: 3K9958V90M) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PPG-5-CETETH-20 (UNII: 4AAN25P8P4) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) PEG/PPG-20/6 DIMETHICONE (UNII: PWZ7N4UIKE) CETYL LACTATE (UNII: A7EVH2RK4O) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z) EDETATE DISODIUM (UNII: 7FLD91C86K) SODIUM HYDROXIDE (UNII: 55X04QC32I) GLYCOLIC ACID (UNII: 0WT12SX38S) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) FD&C RED NO. 40 (UNII: WZB9127XOA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0158-8 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 10/01/2009 Labeler - Kenvue Brands LLC (118772437)