Label: AVANT ALCOHOL-FREE INSTANT HAND SANITIZER- benzalkonium chloride solution

  • NDC Code(s): 68306-112-01, 68306-112-02, 68306-112-03, 68306-112-04, view more
    68306-112-05
  • Packager: B4 Ventures LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 28, 2023

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  • Active Ingredient

    Benzalkonium Chloride 0.1%

  • Purpose

    Antimicrobial

  • Use

    For hand sanitizing to decrease bacteria on the skin

  • Warnings

    For external use only.

    Do not use in the eys. In case of eye contact, flush thoroughly with water and seek medical attention.

    Stop use and ask doctor if irritation and redness develop and persists for more than 72 hours.

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

  • Directions

    • Dispense an adequate amount in your palm to cover all surfaces of hands completely.
    • Rub hands together until dry.
    • Supervise children in the use of this product.
  • Inactive Ingredients

    Water, Cocamidopropyl PG-Dimonium Chloride Phosphate, Dihydroxyethyl Cocamine Oxide, Acetamidoethoxyethanol, Citric Acid

  • Questions or Comments?

    1-888-667-6066 or www.b4brands.com

  • PRINCIPAL DISPLAY PANEL

    Product Label - 18 fl. oz. Table Top Foamer

  • INGREDIENTS AND APPEARANCE
    AVANT ALCOHOL-FREE INSTANT HAND SANITIZER 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68306-112
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 g  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
    ACETAMIDOETHOXYETHANOL (UNII: LVX2APC4XR)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Colorwhite (water white - colorless, dispensed as a white foam) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68306-112-01530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/01/2012
    2NDC:68306-112-021000 mL in 1 POUCH; Type 0: Not a Combination Product01/01/2012
    3NDC:68306-112-032000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product01/01/2012
    4NDC:68306-112-041000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product01/01/2012
    5NDC:68306-112-053785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/27/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/01/2012
    Labeler - B4 Ventures LLC (133582853)
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