AVANT FOAMING HAND SANITIZER- alcohol liquid 
B4 Ventures LLC

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B4 Brands: Avant Foaming Hand Sanitizer - Fragrance Free

Active Ingredient

Ethanol 62% v/v

Purpose

Antimicrobial

Uses

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

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

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

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)

Revised: 11/2023
Document Id: 0ab00ee0-4d1d-8f03-e063-6294a90a351b
Set id: 6cc57ff1-e49b-4c15-b997-886a29d3fe1c
Version: 8
Effective Time: 20231121
 
B4 Ventures LLC