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

Drug Label Information

Updated December 27, 2024

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  • ACTIVE INGREDIENT

    DRUG FACTS

    Active Ingredients........... Salicylic Acid 2%

  • PURPOSE

    Purpose ............... Acne Treatment

  • INDICATIONS & USAGE

    Uses: For the treatment of acne. Penetrates pores to eliminate most acne blemishes, whiteheads & blackheads. Helps prevent new acne blemishes, whiteheads & blackheads.

  • DOSAGE & ADMINISTRATION

    Directions:  Lather with water and massage onto affected areas. Let sit for 30 to 60 seconds to maximize results. Rinse clean with warm water.

  • WARNINGS

    Warnings: For external use only. When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children. If swallowed get medical help or contact a Poison Control center right away.

  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS: WATER/AQUA/EAU, SODIUM C14-16 OLEFIN SULFONATE, COCAMIDOPROPYL HYDROXYSULTAINE, DISTEARETH-75 IPDI, PROPANEDIOL, SODIUM LAUROAMPHOACETATE, GLYCERIN, GLYCOLIC ACID, COCAMIDOPROPYL BETAINE, PHENOXYETHANOL, SODIUM CHLORIDE, GLUCO-NOLACTONE, SODIUM HYDROXIDE, SODIUM GLUCONATE

  • Geologie Clear System Package Labeling

    Geologie

    CLEAR SYSTEM

    Acne Control

    Superclean

    Body Wash

    250 mL  8.4 fl oz

    Geologie.com

    Distributed by Geologie

    New York, NY 10163

    170-50 Geologie

    res

  • INGREDIENTS AND APPEARANCE
    ACNE CONTROL SUPERCLEAN BODY WASH  AHA BHA FORMULA
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54111-170
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2.0 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54111-170-50250 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00603/01/2023
    Labeler - Bentley Laboratories, LLC (068351753)
    Registrant - Geologie (081158549)
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