Label: ANTIBACTERIAL FOAM- benzalkonium chloride solution

  • NDC Code(s): 11084-021-05, 11084-021-42, 11084-021-55
  • Packager: SC Johnson Professional USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 16, 2024

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  • Active ingredient

    BENZALKONIUM CHLORIDE, 0.13%

  • Purpose

    Antibacterial

  • Uses

    for handwashing to reduce bacteria on the skin

  • Warnings

    For external use only

    When using this product

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

    Stop use and ask a doctor if

    irritation and redness develop and persist for more than 3 days.

    Keep out of reach of children.

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

  • Directions

    apply foaming cleanser to dry hands
    rub hands together to spread lather
    wash for 15-20 seconds
    rinse & dry hands thoroughly

  • Inactive ingredients

    AQUA (WATER), GLYCERIN, LAURAMINE OXIDE, BUTYLENE GLYCOL, LACTIC ACID, SALICYLIC ACID, PARFUM (FRAGRANCE), GREEN 5 (CI 61570), YELLOW 5 (CI 19140).

  • PRINCIPAL DISPLAY PANEL

    TSFG1-DCN9290 TOTO 1gal Label-v10.jpg

    TSFG1-DCN9290 TOTO 1gal Label-v10.jpg

    This product does not contain any prop65 ingredients.

    TSFG1

    DCN9290

    TOTO

    Antibacterial Foam Soap

    Cleans hands!

    Kills germs!

    Moisturizes!

    Triclosan-free!

    One Gallon (3.78 Liters)

    Product Features

    A high-quality , softly-perfumed, green foam soap that is 99.99% effective against common bacteria.

    This product contains moisturizers and emollients for the skin making it ideal for frequent use environments.

    Manufactured for:

    TOTO USA, Inc.

    1155 Southern Road

    Morrow, GA 30260

    888-295-8134

    Made in the USA

    R00

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL FOAM 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-021
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11084-021-053.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/01/2017
    2NDC:11084-021-4218.93 L in 1 PAIL; Type 0: Not a Combination Product08/01/201712/31/2024
    3NDC:11084-021-55208.20 L in 1 DRUM; Type 0: Not a Combination Product08/01/201712/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drug505G(a)(3)08/01/2017
    Labeler - SC Johnson Professional USA, Inc. (607378015)
    Establishment
    NameAddressID/FEIBusiness Operations
    APEX International, Inc.015226132manufacture(11084-021)
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