Label: SCOTT ANTISEPTIC FOAM SKIN CLEANSER- chloroxylenol solution

  • NDC Code(s): 55118-900-10, 55118-900-12, 55118-900-63, 55118-900-65
  • Packager: Kimberly-Clark
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Chloroxylenol 1.75 % w/w

  • Purpose

    Antiseptic skin cleanser

  • Use

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

  • Warnings

    For external use only

    Do not use if you are allergic to any of the ingredients.

    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

    Water, Hexylene Glycol, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Disodium EDTA, Sodium Hydroxide, Methylchloroisothiazolinone, Methylisothiazolinone

  • Questions?

    Call 1-888-346-4652

  • SPL UNCLASSIFIED SECTION

    Imported and distributed in Canada by
    Kimberly-Clark Inc., Mississauga, Ontario L5B 3Y5

  • PRINCIPAL DISPLAY PANEL - 1 L Bottle Label

    91555

    Scott®
    Brand

    Antiseptic
    Foam Skin Cleanser

    Chloroxylenol Solution

    RINSE OFF

    Empty &
    Discard Pump
    PLASTIC
    BOTTLE
    how2recycle.info

    For Personal / Domestic Use Only

    20-14-714-0-03

    1 L (33.8 fl oz)

    PRINCIPAL DISPLAY PANEL - 1 L Bottle Label
  • INGREDIENTS AND APPEARANCE
    SCOTT ANTISEPTIC FOAM SKIN CLEANSER 
    chloroxylenol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-900
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Chloroxylenol (UNII: 0F32U78V2Q) (Chloroxylenol - UNII:0F32U78V2Q) Chloroxylenol17.5 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55118-900-636 in 1 CARTON11/16/2018
    1NDC:55118-900-101 L in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:55118-900-652 in 1 CARTON11/16/2018
    2NDC:55118-900-121.2 L 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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