Label: SCOTT ANTIMICROBIAL FOAM SKIN CLEANSER- benzalkonium chloride solution

  • NDC Code(s): 55118-800-10, 55118-800-12, 55118-800-15, 55118-800-63, view more
    55118-800-65, 55118-800-66
  • Packager: Kimberly-Clark
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 11, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Benzalkonium chloride 0.1 % w/w

  • Purpose

    Antiseptic skin cleanser

  • Use

    For personal hand hygiene to help prevent the spread of bacteria.

  • Warnings

    For external use only

    When using this product avoid contact with eyes. If contact occurs, rinse with water.

    Stop use and ask a doctor if irritation develops.

    Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away.

  • Directions

    For occasional and personal domestic use. Supervise children when they use this product. Lather in hands with water for at least 30 seconds. Rinse well.

  • Inactive ingredients

    Aloe Barbadensis Leaf Juice Powder, Citric Acid, Coco-Betaine, Glycerin, Panthenol, Sodium Benzoate, Sodium Chloride, Sodium Hydroxide, Tocopheryl Acetate, Water

  • Questions?

    Call 1-888-346-4652

  • SPL UNCLASSIFIED SECTION

    Distributed in the U.S. by Kimberly-Clark Global Sales,
    LLC, Roswell, GA 30076-2199
    Distributed in Canada by Kimberly-Clark Inc., Mississauga,
    Ontario L5B 3Y5

  • PRINCIPAL DISPLAY PANEL - 1.5 L Bottle Label

    11279

    Scott®
    Brand

    Antimicrobial
    Foam Skin Cleanser

    Benzalkonium Chloride Solution, USP

    RINSE OFF

    Empty &
    Discard Pump

    PLASTIC

    BOTTLE

    how2recycle.info

    DIN 02480816

    For Personal / Domestic Use Only

    1.5 L (50.7 fl oz)

    PRINCIPAL DISPLAY PANEL - 1.5 L Bottle Label
  • INGREDIENTS AND APPEARANCE
    SCOTT ANTIMICROBIAL FOAM SKIN CLEANSER 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-800
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride1 mg  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    Aloe (UNII: V5VD430YW9)  
    Citric Acid Monohydrate (UNII: 2968PHW8QP)  
    Coco-Betaine (UNII: 03DH2IZ3FY)  
    Glycerin (UNII: PDC6A3C0OX)  
    Panthenol (UNII: WV9CM0O67Z)  
    Sodium Benzoate (UNII: OJ245FE5EU)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55118-800-636 in 1 CARTON11/16/2018
    1NDC:55118-800-101000 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:55118-800-652 in 1 CARTON11/16/2018
    2NDC:55118-800-121200 mL in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:55118-800-662 in 1 CARTON11/16/2018
    3NDC:55118-800-151500 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM00311/16/2018
    Labeler - Kimberly-Clark (830997032)
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