Label: AVANT FOAMING HAND SANITIZER- alcohol liquid

  • NDC Code(s): 68306-109-01, 68306-109-02, 68306-109-03
  • Packager: B4 Ventures LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 21, 2023

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  • Active Ingredient

    Ethanol 62% v/v

  • Purpose

    Antimicrobial

  • Uses

    • Hand sanitizer to help reduce bacteria on the skin
    • Recommended for repeated use
  • Warnings

    For external use only.

    Flammable, keep away from fire or flame.

    When using this product do not use in or near eyes. In case of eye contact, flush thoroughly with water.

    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.

  • Other Information

    • Do not store above 100 ºF (38 ºC)
    • May discolor some fabrics
  • Inactive Ingredients

    Water, Acrylates/Perfluorohexylethyl Methacrylate Copolymer, Perfluorohexylethyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice

  • Questions or comments?

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

  • PRINCIPAL DISPLAY PANEL

    Package Label - Front - 1000 mL CartridgePackage Label - Back - 1000 mL Cartridge

  • INGREDIENTS AND APPEARANCE
    AVANT FOAMING HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68306-109
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    2-(PERFLUOROHEXYL)ETHANOL (UNII: G2R5YO5N3V)  
    WATER (UNII: 059QF0KO0R)  
    BUTYL ACRYLATE/METHYL METHACRYLATE/PERFLUOROHEXYLETHYL METHACRYLATE COPOLYMER (SALUS AF) (UNII: HLB263IJK9)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Product Characteristics
    Colorwhite (water white - colorless, dispensed as white foam) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68306-109-01530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/08/2010
    2NDC:68306-109-021000 mL in 1 POUCH; Type 0: Not a Combination Product12/08/2010
    3NDC:68306-109-031000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product05/01/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/08/2010
    Labeler - B4 Ventures LLC (133582853)
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