AVANT ORIGINAL - FRAGRANCE FREE- alcohol gel

Avant Original - Fragrance Free by

Drug Labeling and Warnings

Avant Original - Fragrance Free 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 60%

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 100 degrees F.  Non-staining.  May discolor some fabrics.

Other Ingredients:

Water, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrytate Crosspolymer, Triethanolamine.

Questions or Comments?

  888-667-6066    www.b4brands.com

Package Labeling:

INGREDIENTS AND APPEARANCE

AVANT ORIGINAL - FRAGRANCE FREE 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68306-106
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER 1342 (UNII: 809Y72KV36)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68306-106-02	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/15/2010
2	NDC: 68306-106-01	82.5 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/15/2010
3	NDC: 68306-106-03	1000 mL in 1 POUCH; Type 0: Not a Combination Product	05/15/2010
4	NDC: 68306-106-04	60 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/15/2010
5	NDC: 68306-106-05	120 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/15/2010
6	NDC: 68306-106-06	1920 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/15/2010
7	NDC: 68306-106-08	3785 mL in 1 JUG; Type 0: Not a Combination Product	05/15/2010
8	NDC: 68306-106-10	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	05/15/2010

Labeler - B4 Ventures LLC (133582853)

Registrant - B4 Ventures LLC (133582853)