Label: CLEAN AND CLEAR ACNE EXFOLIATING CLEANSER- salicylic acid liquid
- NDC Code(s): 69968-0822-5
- Packager: Johnson & Johnson Consumer Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 8, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only.
- Directions
- Other Information
-
Inactive ingredients
Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Sorbitol, Cellulose, Sodium Hydrolyzed Potato Starch Dodecenylsuccinate, Glycerin, Aloe Brabadensis Leaf Extract, Mentha Piperita (Peppermint) Leaf Extract, Acrylates Crosspolymer-4, C12-15 Alkyl Lactate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Sodium Hydroxide, Disodium EDTA, Benzalkonium Chloride, Menthol, Fragrance
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 148 mL Tube Label
-
INGREDIENTS AND APPEARANCE
CLEAN AND CLEAR ACNE EXFOLIATING CLEANSER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0822 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 ALOE VERA LEAF (UNII: ZY81Z83H0X) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) ACRYLATES CROSSPOLYMER-4 (UNII: GEV2EL4D9G) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) POWDERED CELLULOSE (UNII: SMD1X3XO9M) SODIUM HYDROXIDE (UNII: 55X04QC32I) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) MENTHA PIPERITA LEAF (UNII: A389O33LX6) SORBITOL (UNII: 506T60A25R) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) MENTHOL (UNII: L7T10EIP3A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0822-5 148 mL in 1 TUBE; Type 0: Not a Combination Product 11/29/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 11/29/2023 Labeler - Johnson & Johnson Consumer Inc. (118772437)