AVANT ALCOHOL-FREE INSTANT HAND SANITIZER- benzalkonium chloride gel

Avant Alcohol-Free Instant Hand Sanitizer by

Drug Labeling and Warnings

Avant Alcohol-Free Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by B4 Ventures, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

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 eyes. 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

• Dispense an adequate amount in to your palm to cover all surfaces of hands completely.
• Rub hands together until dry.
• Supervise children in the use of this product.

Inactive ingredients

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocoate, Citric Acid.

Questions or comments?

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

Package Labeling:

INGREDIENTS AND APPEARANCE

AVANT ALCOHOL-FREE INSTANT HAND SANITIZER 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68306-112
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68306-112-01	530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2012
2	NDC: 68306-112-02	1000 mL in 1 POUCH; Type 0: Not a Combination Product	01/01/2012
3	NDC: 68306-112-03	2000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product	01/01/2012
4	NDC: 68306-112-04	1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product	01/01/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/01/2012

Labeler - B4 Ventures, LLC (133582853)