Label: RELIANCE HAND SANIZITER- benzalkonium chloride solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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.

Drug Label Information

Updated June 1, 2023

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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 not finalpart333E03/30/2011
    Labeler - Ecolab Inc. (006154611)
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