Label: AVANT ECO-PREMIUM INSTANT HAND SANITIZER- alcohol gel

  • NDC Code(s): 68306-114-01, 68306-114-02, 68306-114-03, 68306-114-04, view more
    68306-114-05, 68306-114-06, 68306-114-07
  • Packager: B4 Ventures LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 14, 2019

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active ingredient

    Ethanol 70%

    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 100F (38C)
    • May discolor some fabrics
  • Inactive ingredients

    Water (Aqua), Isopropyl Alcohol, Accrylates/C10-30 Alkyl Acrylate Crosspolymer, Glycerin, Aloe Barbadensis Leaf Juice, Panthenol, Aminomethyl Propanol

  • Questions or comments?

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

  • Package Labeling:

    251 ml Pump Bottle

  • INGREDIENTS AND APPEARANCE
    AVANT ECO-PREMIUM INSTANT HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68306-114
    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)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68306-114-01118 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/01/2012
    2NDC:68306-114-02251 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2012
    3NDC:68306-114-03500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2012
    4NDC:68306-114-041890 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2012
    5NDC:68306-114-051000 mL in 1 POUCH; Type 0: Not a Combination Product05/01/2012
    6NDC:68306-114-061000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/01/2012
    7NDC:68306-114-073785 mL in 1 JUG; Type 0: Not a Combination Product05/01/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/01/2012
    Labeler - B4 Ventures LLC (133582853)
    Registrant - B4 Ventures LLC (133582853)