Label: PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT- benzalkonium chloride wipe cloth

  • NDC Code(s): 21749-359-10, 21749-359-15, 21749-359-20, 21749-359-40
  • Packager: GOJO Industries, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2024

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  • Active ingredient

    Benzalkonium Chloride 0.13%

  • 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

    • Wet hands thoroughly with product and allow to dry

    • Children under 6 years of age should be supervised when using PURELL

  • Inactive ingredients

    Water (Aqua), Decyl Glucoside, Glycerin, Fragrance(Parfum), Phenoxyethanol

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT 
    benzalkonium chloride wipe cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-359
    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)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-359-1010 in 1 PACKAGE08/01/201402/28/2025
    137 mL in 1 PACKAGE; Type 0: Not a Combination Product
    2NDC:21749-359-1515 in 1 PACKAGE08/01/201402/02/2020
    264 mL in 1 PACKAGE; Type 0: Not a Combination Product
    3NDC:21749-359-2020 in 1 PACKAGE08/01/2014
    374 mL in 1 PACKAGE; Type 0: Not a Combination Product
    4NDC:21749-359-4040 in 1 PACKAGE08/01/2014
    4173 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/01/2014
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-359)
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