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Zaliex ALCOHOL-FREE Antiseptic Hand Sanitizer (SAS Healthcare Inc)

Available Formats

Dosage Form Package Information Links
LIQUID 50 mL in 1 BOTTLE (76452-001-00) Label Information

Complete Zaliex ALCOHOL-FREE Antiseptic Hand Sanitizer Information

  • Drug Facts



  • 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.

    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
    • Rub hands together briskly until dry

  • Inactive Ingredients:

    Water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance (parfum)


  • Manufactured for:

    Zaliex

    Suite 210, 4 Robert Speck Parkway,

    Mississauga, Ontario, L4Z1S1, Canada


  • Zaliex ALCOHOL-FREE Antiseptic Foam Hand Sanitizer 50ml

    MOISTURIZES * LEAVES SKIN SOFT


    Zaliex
    ALCOHOL-FREE
    Antiseptic Foam
    HAND SANITIZER

    Eliminates 99.999%
    Of Most Common Germs That May Cause Illness

    1.75 fl oz (50 ml)
    Environmentally Friendly

    Zaliex50ml



  • INGREDIENTS AND APPEARANCE
    ZALIEX ALCOHOL-FREE ANTISEPTIC HAND SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:76452-001
    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 mL  in 100 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:76452-001-00 50 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 10/26/2011
    Labeler - SAS Healthcare Inc (248055696)
    Establishment
    Name Address ID/FEI Business Operations
    Artemis Bio-Solutions Inc. 963442541 manufacture