Label: ACNE CONTROL SUPERCLEAN BODY WASH AHA BHA FORMULA- salicylic acid gel
- NDC Code(s): 54111-170-50
- Packager: Bentley Laboratories, LLC
- 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 March 2, 2023
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INACTIVE INGREDIENT
- Geologie Clear System Package Labeling
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INGREDIENTS AND APPEARANCE
ACNE CONTROL SUPERCLEAN BODY WASH AHA BHA FORMULA
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54111-170 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2.0 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) DISTEARETH-75 ISOPHORONE DIISOCYANATE (UNII: 5365FJ30SC) PROPANEDIOL (UNII: 5965N8W85T) SODIUM LAUROAMPHOACETATE (UNII: SLK428451L) GLYCERIN (UNII: PDC6A3C0OX) GLYCOLIC ACID (UNII: 0WT12SX38S) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM CHLORIDE (UNII: 451W47IQ8X) GLUCONOLACTONE (UNII: WQ29KQ9POT) SODIUM HYDROXIDE (UNII: 55X04QC32I) SODIUM GLUCONATE (UNII: R6Q3791S76) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54111-170-50 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 03/01/2023 Labeler - Bentley Laboratories, LLC (068351753) Registrant - Geologie (081158549)