AVANT ORIGINAL INSTANT HAND SANITIZER- alcohol gel

Avant Original Instant Hand Sanitizer by

Drug Labeling and Warnings

Avant Original 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]

Bio-Based Hand Sanitizer

Avant Original Instant Hand Sanitizer is bio-based and part of B4 Brands' family of environmentally sensitive products.  Avant Original contains 60% grain based ethanol and other natural ingredients, making it more environmentally sensitive than petroleum based products.

Learn more about our products at www.b4brands.com

ACTIVE INGREDIENT

Ethanol 60%

Purpose

Antiseptic

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.
  

STOP USE

• If irritation develops, discontinue use.  If condition persists, consult a physician.
  

KEEP OUT OF REACH OF CHILDREN

• Keep out of reach of children.
  

STORAGE AND HANDLING

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

Other Ingredients:

Water, Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Fragrance, Tocopheryl Acetate, Retinyl Palmitate.

QUESTIONS

Question or Comments?  888-667-6066    www.b4brands.com

PRINCIPAL DISPLAY PANEL

251 ml Pump Bottle

DOSAGE & ADMINISTRATION

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

INDICATIONS & USAGE

For hand sanitizing when soap and water are not available.

INGREDIENTS AND APPEARANCE

AVANT ORIGINAL INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68306-101
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)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68306-101-04	80 mL in 1 BOTTLE, DISPENSING
2	NDC: 68306-101-06	500 mL in 1 BOTTLE, PUMP
3	NDC: 68306-101-07	1000 mL in 1 POUCH
4	NDC: 68306-101-05	251 mL in 1 BOTTLE, PUMP
5	NDC: 68306-101-01	3784 mL in 1 BOTTLE
6	NDC: 68306-101-02	208120 mL in 1 DRUM

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/05/2010

Labeler - B4 Ventures LLC (133582853)

Registrant - B4 Ventures LLC (133582853)