Label: NEUTROGENA RAPID CLEAR ACNE ELIMINATING SPOT- salicylic acid gel
- NDC Code(s): 69968-0472-1
- Packager: Johnson & Johnson Consumer Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 6, 2023
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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 final part333D 10/30/2019 Labeler - Johnson & Johnson Consumer Inc. (118772437)