ZALIEX ALCOHOL-FREE ANTISEPTIC HAND SANITIZER- benzalkonium chloride liquid

Zaliex Alcohol-Free Antiseptic Hand Sanitizer by

Drug Labeling and Warnings

Zaliex Alcohol-Free Antiseptic 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 Antiseptic Foam Hand Sanitizer

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses:

• For hand cleansing to decrease bacteria on the skin
• Recommended for repeated use
  

Warnings:

For external use only.

Do not use in eyes. If contact occurs, flush eyes with water.

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

If condition persists for more than 72 hours, consult a doctor.

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
• Wet hands thoroughly with product and allow to dry without wiping.
  
• 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 Antiseptic Foam Hand Sanitizer 250ml (

76452-003-00) | Zaliex Alcohol-Free Antiseptic Foam Hand Sanitizer 550ml (76452-003-01)

INGREDIENTS AND APPEARANCE

ZALIEX ALCOHOL-FREE ANTISEPTIC HAND SANITIZER  
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76452-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mg  in 1 mL

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: 76452-003-00	250 mL in 1 BOTTLE
2	NDC: 76452-003-01	550 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/13/2012

Labeler - SAS Healthcare Inc (248055696)

Establishment
Name	Address	ID/FEI	Business Operations
Artemis Bio-Solutions Inc.		963442541	manufacture(76452-003)