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

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

ZALIEX ALCOHOL-FREE FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [SAS HEALTHCARE INC]
PDF | XML
NDC 76452-004-00
Set ID 2e80a8ba-9fa9-44b9-849b-ae590d761a2e
Category HUMAN OTC DRUG LABEL
Packager SAS Healthcare Inc
Generic Name
Product Class
Product Number
Application Number PART333E
View All Sections
  • 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)

    ZaliexHandSanitizer1000mLFrench


  • INGREDIENTS AND APPEARANCE
    ZALIEX ALCOHOL-FREE FOAMING HAND SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76452-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 mg  in 0.001 L
    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:76452-004-001 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/FEIBusiness Operations
    Artemis Bio-Solutions Inc.963442541manufacture(76452-004)
View All Sections

Related Drugs

Search DailyMed Drugs