Label: ACNE CONTROL BODY WASH- salicylic acid gel

  • NDC Code(s): 54111-184-01
  • Packager: Bentley Laboratories, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 28, 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 IPDI,
    PROPANEDIOL, SODIUM LAUROAMPHOACETATE,
    GLYCERIN, COCAMIDOPROPYL BETAINE, GLYCOLIC
    ACID, PHENOXYETHANOL, SODIUM HYDROXIDE,
    GLUCONOLACTONE, SODIUM GLUCONATE, FRAGRANCE
    PARFUM, BLUE 1 (CI 42090), SODIUM CHLORIDE

  • Geologie Acne Control Body Wash Labeling

    Acne Control
    Body Wash
    FRESH EUCALYPTUS


    2% Salicylic Acid
    1.5% Glycolic Acid

    8.4 fl oz | 250 ml

    Geologie.com
    Made in USA of
    Global Materials
    Distributed by Geologie
    2578 Broadway #A212
    New York, NY 10025

    184 Wash

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  • INGREDIENTS AND APPEARANCE
    ACNE CONTROL BODY WASH 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54111-184
    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 IPDI (UNII: 5365FJ30SC)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    BLUE 1 (UNII: H3R47K3TBD)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54111-184-01250 mL in 1 BOTTLE; Type 0: Not a Combination Product12/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00612/01/2024
    Labeler - Bentley Laboratories, LLC (068351753)
    Registrant - Geologie (081158549)
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