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Scott (Kimberly-Clark Corporation)

Available Formats

Dosage Form Package Information Links
SOLUTION 3785 mL in 1 BOTTLE, PLASTIC (55118-225-01) Label Information
SOLUTION 800 mL in 1 BAG (55118-225-08) Label Information

Complete Scott Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active Ingredient

    Chloroxylenol 0.5%


  • Purpose

    Antiseptic


  • Use

    For handwashing to decrease bacteria on the skin.


  • Warnings

    For External Use Only.

    When using this product avoid contact with eyes; in case of contact, flush eyes with water.

    Stop use & ask a doctor If irritation or redness develops and persists.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.


  • Directions

    Wet hands and apply a palmful to hands. Scrub thoroughly for 15-20 seconds.

    Rinse and dry thoroughly.


  • Other Information

    • Report serious side effects from this product to 1-877-561-6587

  • Inactive Ingredients

    Water, Sodium Laureth Sulfate, Sodium Chloride, Cocamidopropyl Betaine, Propylene Glycol, Fragrance, Ethanolamine, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone


  • Questions?

    1-888-346-4652


  • SPL UNCLASSIFIED SECTION

    Distributed in the U.S. by
    Kimberly-Clark Global Sales, LLC,
    Roswell, GA 30076-2199


  • PRINCIPAL DISPLAY PANEL - 800 mL Container Label

    91298

    Scott*
    BRAND

    Antibacterial Skin Cleanser

    Chloroxylenol 0.5%

    DIN: XXXXXXXX

    800 mL (27 fl oz)

    PRINCIPAL DISPLAY PANEL - 800 mL Container Label

  • INGREDIENTS AND APPEARANCE
    SCOTT   ANTIBACTERIAL SKIN CLEANSER
    chloroxylenol solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:55118-225
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Chloroxylenol (UNII: 0F32U78V2Q) (Chloroxylenol - UNII:0F32U78V2Q) Chloroxylenol 0.5 g  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    Water (UNII: 059QF0KO0R)  
    Sodium Laureth-3 Sulfate (UNII: BPV390UAP0)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
    Coco Diethanolamide (UNII: 92005F972D)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Monoethanolamine (UNII: 5KV86114PT)  
    Citric Acid Monohydrate (UNII: 2968PHW8QP)  
    Methylchloroisothiazolinone (UNII: DEL7T5QRPN)  
    Methylisothiazolinone (UNII: 229D0E1QFA)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:55118-225-08 800 mL in 1 BAG; Type 0: Not a Combination Product
    2 NDC:55118-225-01 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part333E 03/01/2012
    Labeler - Kimberly-Clark Corporation (006072136)