Label: CLEAN AND CLEAR ADVANTAGE ACNE SPOT TREATMENT- salicylic acid lotion
- NDC Code(s): 69968-0126-1
- 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
Alcohol Denat., Water, 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 - 22 mL Tube Carton
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INGREDIENTS AND APPEARANCE
CLEAN AND CLEAR ADVANTAGE ACNE SPOT TREATMENT
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0126 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 WATER (UNII: 059QF0KO0R) WITCH HAZEL (UNII: 101I4J0U34) 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) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ) SARCOSINE (UNII: Z711V88R5F) CINNAMON BARK OIL (UNII: XE54U569EC) CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF) PURSLANE (UNII: M6S840WXG5) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0126-1 1 in 1 CARTON 10/01/2006 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 10/01/2006 Labeler - Kenvue Brands LLC (118772437)