ZALIEX ALCOHOL-FREE FOAMING HAND SANITIZER- benzalkonium chloride liquid

Zaliex Alcohol-Free Foaming Hand Sanitizer by

Drug Labeling and Warnings

Zaliex Alcohol-Free Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by SAS Healthcare Inc, Artemis Bio-Solutions Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Zaliex Alcohol-Free Foaming Hand Sanitizer

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses:

For hand sanitizing, to eliminate harmful bacteria and germs on skin.
Use as part of your daily cleansing routine.
Recommended for repeated use.

Warnings:

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

• Pump a small amount of foam into palm of hand
• Run thoroughly over all surfaces of both hands
• Rub hands together briskly until dry
  

Inactive Ingredients:

Water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance

Manufactured for:

Zaliex

Suite 210, 4 Robert Speck Parkway,

Mississauga, Ontario, L4Z1S1, Canada

Zaliex Alcohol-Free Foaming Hand Sanitizer 1L (

76452-004-00)

INGREDIENTS AND APPEARANCE

ZALIEX ALCOHOL-FREE FOAMING HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76452-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 mg  in 0.001 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76452-004-00	1 L in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/26/2011

Labeler - SAS Healthcare Inc (248055696)

Establishment
Name	Address	ID/FEI	Business Operations
Artemis Bio-Solutions Inc.		963442541	manufacture(76452-004)