AVANT FOAMING HAND SANITIZER- alcohol liquid

Avant Foaming Hand Sanitizer by

Drug Labeling and Warnings

Avant Foaming 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

Ethanol 62%

Purpose

Antiseptic

Indications:

For use as a healthcare personnel hand antiseptic to reduce risk of disease transfer.

Directions:

Dispense an adequate amount in your palm to cover all surfaces of hands completely. Rub hands together until dry. Does not require rinsing.

Warnings:

• FOR EXTERNAL USE ONLY.
• FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.
• Keep away from eyes. In case of eye contact, flush thoroughly with water and then seek medical advice.
• If swallowed, drink large amounts of water and seek medical attention.
• Avoid contact with face and broken skin. If contact occurs, flush with water.
• If irritation develops, discontinue use. If condition persists, consult a physician.

Keep out of the reach of children.

Note:

Do not store above 100F. Non-staining. May discolor some fabrics.

Other Ingredients:

Water, DEA-C8-18 Perfluoroalkylethyl, Glycerin, Propylene-Glycol, Aloe Barbadensis Leaf Juice, Citric Acid.

Questions or Comments?

 888-667-6066       www.b4brands.com

PRINCIPAL DISPLAY PANEL

530 ml Pump Bottle

INGREDIENTS AND APPEARANCE

AVANT FOAMING HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68306-109
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68306-109-01	530 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/08/2010
2	NDC: 68306-109-02	1000 mL in 1 POUCH; Type 0: Not a Combination Product	12/08/2010
3	NDC: 68306-109-03	1000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product	05/01/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	12/08/2010

Labeler - B4 Ventures LLC (133582853)

Registrant - B4 Ventures LLC (133582853)