Label: CLEAN AND CLEAR ACNE SPOT TREATMENT- salicylic acid gel
- NDC Code(s): 69968-0804-1
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 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 open 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.
- Other Information
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Inactive Ingredients
Water, Alcohol Denat., Hamamelis Virginiana(Witch Hazel) Water, Polyacrylamide, Glycerin, C13-14 Isoparaffin, C12-15 Alkyl Lactate, Alcohol, Phenoxyethanol, Cetyl Lactate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Laureth-7, Polysorbate 20, Sodium Hydroxide, Phenethyl Dimethicone, Xanthan Gum, Propylene Glycol, Benzalkonium Chloride, Tetrasodium EDTA
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 22 mL Tube Carton
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INGREDIENTS AND APPEARANCE
CLEAN AND CLEAR ACNE SPOT TREATMENT
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0804 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 C12-15 ALKYL LACTATE (UNII: GC844VRD7E) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) EDETATE SODIUM (UNII: MP1J8420LU) WATER (UNII: 059QF0KO0R) LAURETH-7 (UNII: Z95S6G8201) CETYL LACTATE (UNII: A7EVH2RK4O) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) POLYSORBATE 20 (UNII: 7T1F30V5YH) SODIUM HYDROXIDE (UNII: 55X04QC32I) ALCOHOL (UNII: 3K9958V90M) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) GLYCERIN (UNII: PDC6A3C0OX) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) XANTHAN GUM (UNII: TTV12P4NEE) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0804-1 1 in 1 CARTON 11/13/2023 1 22 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 11/13/2023 Labeler - Kenvue Brands LLC (118772437)