Label: NEUTROGENA STUBBORN BODY ACNE TREATMENT- salicylic acid spray
- NDC Code(s): 69968-0758-6
- 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. Flammable: Keep away from fire or flame.
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Directions
■ Clean the 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.
- Inactive ingredients
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Other information
- Store at room temperature.
- 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.
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 186 mL Bottle Label
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INGREDIENTS AND APPEARANCE
NEUTROGENA STUBBORN BODY ACNE TREATMENT
salicylic acid sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0758 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 ALCOHOL (UNII: 3K9958V90M) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SODIUM CITRATE (UNII: 1Q73Q2JULR) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) WATER (UNII: 059QF0KO0R) PPG-5-CETETH-20 (UNII: 4AAN25P8P4) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) CETYL LACTATE (UNII: A7EVH2RK4O) SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) SODIUM HYDROXIDE (UNII: 55X04QC32I) GLYCOLIC ACID (UNII: 0WT12SX38S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0758-6 162 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 08/01/2022 Labeler - Kenvue Brands LLC (118772437)