Label: NEUTROGENA RAPID CLEAR- salicylic acid swab
- NDC Code(s): 10812-204-01
- 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 24, 2023
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- Download DRUG LABEL INFO: PDF XML
- 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
- 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 applications to once a day or every other day.
- Other information
- Sunburn Alert
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 60 Pad Jar Label
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INGREDIENTS AND APPEARANCE
NEUTROGENA RAPID CLEAR
salicylic acid swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10812-204 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 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) SODIUM HYDROXIDE (UNII: 55X04QC32I) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) CETYL LACTATE (UNII: A7EVH2RK4O) EDETATE DISODIUM (UNII: 7FLD91C86K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10812-204-01 60 in 1 JAR; Type 0: Not a Combination Product 02/09/2010 07/11/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 02/09/2010 07/11/2024 Labeler - Johnson & Johnson Consumer Inc. (118772437)