Label: SCOTT FOAM HAND SANITIZER- benzalkonium chloride solution

  • NDC Code(s): 55118-664-10, 55118-664-12, 55118-664-63, 55118-664-65
  • Packager: Kimberly-Clark
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Benzalkonium chloride 0.13 % 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. Rub thoroughly into hands for at least 30 seconds. Allow to dry.

  • Inactive ingredients

    Aloe Barbadensis Leaf Juice Powder, Citric Acid, Cocoamidopropyl PG-Dimonium Chloride Phosphate, Methylpropanediol, Panthenol, Polyethylene Glycol, Silica, Sodium Hydroxide, Water

  • 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

    12977

    Scott®
    Brand

    Foam Hand Sanitizer

    Benzalkonium Chloride Solution, USP

    Alcohol free

    LEAVE ON

    Empty &
    Discard Pump
    PLASTIC
    BOTTLE
    how2recycle.info

    DIN 02481456

    For Personal / Domestic Use Only

    20-14-559-0-07

    1 L (33.8 fl oz)

    PRINCIPAL DISPLAY PANEL - 1 L Bottle Label
  • INGREDIENTS AND APPEARANCE
    SCOTT FOAM HAND SANITIZER 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-664
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride1.3 mg  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    METHYLPROPANEDIOL (UNII: N8F53B3R4R)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    POLYETHYLENE OXIDE 600000 (UNII: 2126FD486L)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55118-664-636 in 1 CARTON11/16/2018
    1NDC:55118-664-101000 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:55118-664-652 in 1 CARTON11/16/2018
    2NDC:55118-664-121200 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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