Label: PURELL SF607 INSTANT HAND SANITIZING- benzalkonium chloride liquid

  • NDC Code(s): 21749-607-31, 21749-607-53, 21749-607-89
  • Packager: GOJO Industries, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 16, 2024

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  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antimicrobial

  • Use

    • Hand sanitizer to help reduce bacteria on the skin
  • Warnings

    For external use only

    When using this productdo not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. 

    Stop use and ask a doctor ifirritation or rash appears and lasts 

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

  • Directions

    • Place enough product in your palm to thoroughly cover your hands
    • Rub hands together briskly until dry
    • Children under 6 years of age should be supervised when using this product.
  • INACTIVE INGREDIENT

    Water (Aqua), Decyl Glucoside, Glycerin, Methylparaben, Phenoxyethanol, Propylparaben

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    PURELL SF607 INSTANT HAND SANITIZING 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-607
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-607-3145 mL in 1 BOTTLE; Type 0: Not a Combination Product01/03/201101/01/2024
    2NDC:21749-607-53535 mL in 1 BOTTLE; Type 0: Not a Combination Product01/03/201101/01/2024
    3NDC:21749-607-891200 mL in 1 BOTTLE; Type 0: Not a Combination Product01/03/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/03/2011
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-607)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414label(21749-607) , pack(21749-607)
    Establishment
    NameAddressID/FEIBusiness Operations
    Travis Association for the Blind026032268label(21749-607)
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