Label: RELIANCE HAND SANIZITER- benzalkonium chloride solution

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated April 26, 2024

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  • Active ingredient

    Benzalkonium chloride 0.1%

  • Purpose

    Antiseptic handwash

  • Uses

    • for handwashing to decrease bacteria on the skin
  • Warnings

    For external use only

    Do not use

    • in eyes

    • if in eyes, rinse promptly and thoroughly with water
    • discontinue use if irritation and redness develop

    Stop use and ask a doctor if

    • skin irritation or redness occurs for more than 72 hours

    Keep our of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

  • Direction

    • wash hands to remove soil
    • dispense palmful
    • spread to cover hands, rub in well
    • air dry, do not rinse or towel dry
  • Other information

    • for additional information, see Material Safety Data Sheet (MSDS)
    • for emergency medical information in USA, call 1.800.328.0026
  • INACTIVE INGREDIENT

    Inactive ingredients water (aqua), isopropyl alcohol, propylene glycol, FDC red 40, FDC blue 1

  • QUESTIONS

    Questions? call 1.800.35.CLEAN (352.5326)

  • Principal display panel and representative label

    SYSCO

    RELIANCE   SUPC 0281495

    SYSCO FOAM HAND SANITIZER

    Active ingredient: Benzalkonium chloride 0.1%

    NET CONTENTS 25.4 US FL OZ (750mL)

    DISTRIBUTED BY SYSCO CORPORATION

    ECOLAB, 370 WABASHA STREET N, ST PAUL,

    MN 55102-1390 USA, TEL. 1 800 352 5326

    001123

    6100593

    751643/5402/0715

    representative label

  • INGREDIENTS AND APPEARANCE
    RELIANCE HAND SANIZITER 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-478
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47593-478-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/30/2011
    Labeler - Ecolab Inc. (006154611)
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