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Zaliex Antiseptic Hand

Dosage form: soap
Ingredients: BENZALKONIUM CHLORIDE 0.13mg in 1mL
Labeler: SAS Healthcare Inc
NDC Code: 76452-002

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 Antiseptic Foam Hand Soap

Zaliex Antiseptic Foam Hand Soap


Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses:
  • For hand washing to decrease bacteria on the skin
  • 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 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:
  • Pump a small amount of foam into palm of hand
  • Run thoroughly over all surfaces of both hands for 15 seconds
  • Rinse with potable water

Inactive Ingredients:

Water (aqua), coco-glucoside, laurtrimonium chloride, cocamidopropylamine oxide.

Manufactured for:

Zaliex

Suite 210, 4 Robert Speck Parkway,

Mississauga, Ontario, L4Z1S1, Canada

Zaliex Antiseptic Foam Hand Soap 250ml | Zaliex Antiseptic Foam Hand Soap 550ml (76452-002-01) | Zaliex Antiseptic Foam Hand Soap 1000ml (76452-002-02) TRICLOSAN FREE


Zaliex
Antiseptic Foam
HAND SOAP

MOISTURIZES * LEAVES SKIN SOFT

Eliminates 99.999%
Of Most Common Germs That May Cause Illness

8.4 fl oz (250 ml)
Environmentally Friendly






ZALIEX ANTISEPTIC HAND 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76452-002
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.13 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
COCO GLUCOSIDE 
COCAMIDOPROPYLAMINE OXIDE 
Packaging
#Item CodePackage Description
1NDC:76452-002-00250 mL in 1 BOTTLE
2NDC:76452-002-01550 mL in 1 BOTTLE
3NDC:76452-002-021000 mL 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(76452-002)

Revised: 09/2012
Document Id: 7318b746-f215-4ac9-9d0e-d2a71658134f
Set id: 262c135c-ac11-4a57-8c2e-85b90f5e2a0d
Version: 4
Effective Time: 20120912
 
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 drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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