ZALIEX ALCOHOL-FREE ANTISEPTIC HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [SAS HEALTHCARE INC]

  • Home
  • ZALIEX ALCOHOL-FREE ANTISEPTIC HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [SAS HEALTHCARE INC]

ZALIEX ALCOHOL-FREE ANTISEPTIC HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [SAS HEALTHCARE INC]
PDF | XML
NDC 76452-003-00, 76452-003-01
Set ID 68028681-572e-450c-a33c-0bb9ad647c1d
Category HUMAN OTC DRUG LABEL
Packager SAS Healthcare Inc
Generic Name
Product Class
Product Number
Application Number PART333E
View All Sections
  • 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)

    ZaliexHandSanitizer250mLFrench

    ZaliexHandSanitizer550mLFrench


  • INGREDIENTS AND APPEARANCE
    ZALIEX ALCOHOL-FREE ANTISEPTIC HAND SANITIZER  
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76452-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76452-003-00250 mL in 1 BOTTLE
    2NDC:76452-003-01550 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/13/2012
    Labeler - SAS Healthcare Inc (248055696)
    Establishment
    NameAddressID/FEIBusiness Operations
    Artemis Bio-Solutions Inc.963442541manufacture(76452-003)
View All Sections

Related Drugs

Search DailyMed Drugs