AVANT ALCOHOL-FREE INSTANT HAND SANITIZER- benzalkonium chloride solution 
B4 Ventures LLC

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Avant Alcohol-Free Foaming Instant Hand Sanitizer

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

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

Product Label - 18 fl. oz. Table Top Foamer

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)

Revised: 11/2023
Document Id: 0b391ae2-97f1-aeed-e063-6294a90a0d16
Set id: ec561e3b-996e-484a-af64-f388f0fbfe5b
Version: 7
Effective Time: 20231128
 
B4 Ventures LLC