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

Drug Label Information

Updated December 16, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • 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)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!