Label: AVANT 70% ALCOHOL GEL- alcohol gel

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

Drug Label Information

Updated November 20, 2023

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  • Active Ingredient

    Ethyl Alcohol 70% 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 ºF).
    • May discolor some fabrics.
  • Inactive Ingredients

    Water, Glycerin, Carbomer, Propylene Glycol, Diisopropylamine

  • Questions or Comments?

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

  • PRINCIPAL DISPLAY PANEL

    Product Label - 55 gallon Drum

  • INGREDIENTS AND APPEARANCE
    AVANT 70% ALCOHOL GEL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68306-116
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIISOPROPYLAMINE (UNII: BR9JLI40NO)  
    Product Characteristics
    Colorwhite (water white - colorless, crystal clear) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68306-116-01208198 mL in 1 DRUM; Type 0: Not a Combination Product01/12/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/12/2023
    Labeler - B4 Ventures LLC (133582853)
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