Label: NEUTROGENA RAPID CLEAR ACNE ELIMINATING SPOT- salicylic acid gel
- NDC Code(s): 69968-0472-1
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
- Warnings
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Directions
- cleanse the skin thoroughly before applying product.
- cover the entire affected area with a thin layer 1-3 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 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 a 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., hamamelis virginiana (witch hazel) water, polyacrylamide, glycerin, cyclopentasiloxane, C13-14 isoparaffin, C12-15 alkyl lactate, alcohol, phenoxyethanol, cetyl lactate, PPG-2 isoceteth-20 acetate, cocamidopropyl PG-dimonium chloride phosphate, laureth-7, polysorbate 20, phenethyl dimethicone, fragrance, dehydroxanthan gum, propylene glycol, benzalkonium chloride, ammonia, tetrasodium EDTA, butylene glycol, capryloyl glycine, sarcosine, cinnamomum zeylanicum bark extract, cedrus atlantica bark extract, portulaca oleracea extract
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 15 mL Tube Carton
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INGREDIENTS AND APPEARANCE
NEUTROGENA RAPID CLEAR ACNE ELIMINATING SPOT
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0472 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 BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ) SARCOSINE (UNII: Z711V88R5F) CINNAMON BARK OIL (UNII: XE54U569EC) CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF) PURSLANE (UNII: M6S840WXG5) WATER (UNII: 059QF0KO0R) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) GLYCERIN (UNII: PDC6A3C0OX) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) ALCOHOL (UNII: 3K9958V90M) PHENOXYETHANOL (UNII: HIE492ZZ3T) CETYL LACTATE (UNII: A7EVH2RK4O) PPG-2 ISOCETETH-20 ACETATE (UNII: BI6C7YO419) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) LAURETH-7 (UNII: Z95S6G8201) POLYSORBATE 20 (UNII: 7T1F30V5YH) DEHYDROXANTHAN GUM (UNII: 63ZP7I1BQO) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) AMMONIA (UNII: 5138Q19F1X) EDETATE SODIUM (UNII: MP1J8420LU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0472-1 1 in 1 CARTON 10/30/2019 1 15 mL in 1 TUBE; 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 10/30/2019 Labeler - Kenvue Brands LLC (118772437)
