AVANT ECO-PREMIUM INSTANT HAND SANITIZER- alcohol gel

Avant Eco-Premium Instant Hand Sanitizer by

Drug Labeling and Warnings

Avant Eco-Premium 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

Ethanol 70%

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 100F (38C)
• May discolor some fabrics
  

Inactive ingredients

Water (Aqua), Isopropyl Alcohol, Accrylates/C10-30 Alkyl Acrylate Crosspolymer, Glycerin, Aloe Barbadensis Leaf Juice, Panthenol, Aminomethyl Propanol

Questions or comments?

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

Package Labeling:

INGREDIENTS AND APPEARANCE

AVANT ECO-PREMIUM INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68306-114
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)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PANTHENOL (UNII: WV9CM0O67Z)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68306-114-01	118 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2012
2	NDC: 68306-114-02	251 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2012
3	NDC: 68306-114-03	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2012
4	NDC: 68306-114-04	1890 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2012
5	NDC: 68306-114-05	1000 mL in 1 POUCH; Type 0: Not a Combination Product	05/01/2012
6	NDC: 68306-114-06	1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/01/2012
7	NDC: 68306-114-07	3785 mL in 1 JUG; 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	05/01/2012

Labeler - B4 Ventures LLC (133582853)

Registrant - B4 Ventures LLC (133582853)