Label: CLEAN AND CLEAR ACNE TRIPLE CLEAR EXFOLIATING SCRUB- salicylic acid gel
- NDC Code(s): 69968-0013-5
- 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 5, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
For external use only.
- Directions
- Other information
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Inactive ingredients
Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Sorbitol, Cellulose, Sodium Hydrolyzed Potato Starch Dodecenylsuccinate, Acrylates Crosspolymer-4, Sodium Hydroxide, Fragrance, Microcrystalline Wax, Menthol, C12-15 Alkyl Lactate, Benzalkonium Chloride, Disodium EDTA, Glycerin, Cocamidopropyl PG-Dimonium Chloride Phosphate, Aloe Barbadensis Leaf Extract, Mentha Piperita (Peppermint) Leaf Extract, Ferric Ferrocyanide
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 141 g Tube Label
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INGREDIENTS AND APPEARANCE
CLEAN AND CLEAR ACNE TRIPLE CLEAR EXFOLIATING SCRUB
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0013 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 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) GLYCERIN (UNII: PDC6A3C0OX) SODIUM HYDROXIDE (UNII: 55X04QC32I) FERRIC FERROCYANIDE (UNII: TLE294X33A) ALOE VERA LEAF (UNII: ZY81Z83H0X) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) POWDERED CELLULOSE (UNII: SMD1X3XO9M) MENTHA PIPERITA LEAF (UNII: A389O33LX6) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) SORBITOL (UNII: 506T60A25R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0013-5 141 g in 1 TUBE; Type 0: Not a Combination Product 11/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 11/01/2016 Labeler - Johnson & Johnson Consumer Inc. (118772437)