Label: BAC-OFF- foaming hand sanitizer aerosol, foam

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

Drug Label Information

Updated January 11, 2024

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  • ACTIVE INGREDIENT

    Active Ingredient:

    Benzalkonium chloride 0.1%................antiseptic antimicrobial

  • PURPOSE

    Non-Alcohol Foaming Hand Sanitizer

    This product is an economical hand sanitizer designed to produce thick, rich foam.

    Non-alcohol formula sanitizes thoroughly and is gentle on hands.

    Removes bacteria while leaving a fresh aloe scent.

    For use with or without water.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • INDICATIONS & USAGE

    Directions

    1. Apply liberally into palm of hand

    2. Rub hands together to spread foam evenly

    3. Allow hands to air dry

  • WARNINGS

    FIRST AID: IF IN EYES: Rinse cautiously with water for several minutes.

    Remove contact lenses, if present and easy to do. Continue rinsing. IF ON SKIN: Wash with plenty of water. IF INHALED: Remove victim to fresh air and keep at rest in a posltion comfortable for breathing. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.

  • DOSAGE & ADMINISTRATION

    Directions

    1. Apply liberally into palm of hand

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, glycerin, surfactant, aloe

  • PRINCIPAL DISPLAY PANEL

    Label

  • INGREDIENTS AND APPEARANCE
    BAC-OFF 
    foaming hand sanitizer aerosol, foam
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76315-1052
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE100 g  in 100 L
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 99000 g  in 100 L
    GLYCERIN (UNII: PDC6A3C0OX) 250 g  in 100 L
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 3   in 100 L
    C12-15 PARETH-10 (UNII: Z0QJT9586T) 250   in 100 L
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76315-1052-13.8 L in 1 JUG; Type 0: Not a Combination Product08/15/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM08/15/2022
    Labeler - DeVere Company, Inc. (006074579)
    Registrant - DeVere Company, Inc. (006074579)
    Establishment
    NameAddressID/FEIBusiness Operations
    DeVere Company, Inc.006074579api manufacture(76315-1052)
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