AVANT 70% ALCOHOL GEL- alcohol gel

Avant 70% Alcohol Gel by

Drug Labeling and Warnings

Avant 70% Alcohol Gel by is a Otc medication manufactured, distributed, or labeled by B4 Ventures LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

AVANT 70% ALCOHOL GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68306-116
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DIISOPROPYLAMINE (UNII: BR9JLI40NO)

Product Characteristics
Color	white (water white - colorless, crystal clear)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68306-116-01	208198 mL in 1 DRUM; Type 0: Not a Combination Product	01/12/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/12/2023

Labeler - B4 Ventures LLC (133582853)