Label: FRESH HAND FOAMING HAND SANITIZER NON-ALCOHOL FOAM- benzalkonium chloride solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 21, 2023

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  • Active ingredient

    BENZALKONIUM CHLORIDE 0.13%

    Purpose

    Antibacterial

  • PURPOSE

    ANTIMICROBIAL

  • Use

    • FOR HANDWASHING TO DECREASE BACTERIA ON THE SKIN. RECOMMENDED FOR REPEATED USE.
  • WARNINGS

    For external use only.

    WARNING: HARMFUL IF SWALLOWED.

    CAUTION: KEEP OUT OF EYES. IN CASE OF ACCIDENTAL EYE CONTACT, FLUSH EYES THOROUGHLY WITH WATER. IF CONDITION WORSENS OR PERSISTS, CONTACT A PHYSICIAN. IF SWALLOWED, CONTACT A PHYSICIAN OR POISON CONTROL CENTER IMMEDIATELY.

    When using this product

    • avoid contact with eyes. In case of eye contact, flush with water

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • DIRECTIONS

    • APPLY FOAM SANITIZER TO HANDS AND RUB OVER SURFACES OF BOTH HANDS FOR 15 SECONDS. NO RINSING REQUIRED.

  • Inactive ingredients

    WATER, COCO-GLUCOSIDE, LAURTRIMONIUM CHLORIDE, COCAMIDOPROPYLAMINE OXIDE, CITRIC ACID, FRAGRANCE.

  • PRINCIPAL DISPLAY PANEL

    01b LBL_Non-Alcohol Foam_Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    FRESH HAND FOAMING HAND SANITIZER NON-ALCOHOL FOAM 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70415-204
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70415-204-111000 mL in 1 BOTTLE; Type 0: Not a Combination Product08/05/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/05/2020
    Labeler - CWGC LA Inc. (034967904)
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