Medication Guide App

Zaliex Alcohol-Free Foaming Hand Sanitizer

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 0.1mg in 0.001L
Labeler: SAS Healthcare Inc
NDC Code: 76452-004

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Zaliex Alcohol-Free Foaming Hand Sanitizer

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)


ZALIEX ALCOHOL-FREE FOAMING HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76452-004
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.1 mg  in 0.001 L
Inactive Ingredients
Ingredient NameStrength
WATER 
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE 
GLYCERETH-2 COCOATE 
BEHENTRIMONIUM CHLORIDE 
DIHYDROXYETHYL COCAMINE OXIDE 
Packaging
#Item CodePackage Description
1NDC:76452-004-001 L in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E10/26/2011
Labeler - SAS Healthcare Inc (248055696)
Establishment
NameAddressID/FEIOperations
Artemis Bio-Solutions Inc.963442541manufacture(76452-004)

Revised: 09/2012
 
SAS Healthcare Inc

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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