PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT (BENZALKONIUM CHLORIDE WIPE) LIQUID [GOJO INDUSTRIES, INC.]

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  • PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT (BENZALKONIUM CHLORIDE WIPE) LIQUID [GOJO INDUSTRIES, INC.]

PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT (BENZALKONIUM CHLORIDE WIPE) LIQUID [GOJO INDUSTRIES, INC.]
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NDC 21749-359-10, 21749-359-15, 21749-359-20, 21749-359-40, 21749-359-70
Set ID 4a8862cd-682f-4419-8f0c-794bae243e65
Category HUMAN OTC DRUG LABEL
Packager GOJO Industries, Inc.
Generic Name
Product Class
Product Number
Application Number PART333E
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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 product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation 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

    40ct 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:21749-359-4040 in 1 PACKAGE08/01/2014
    1173 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/01/2014
    Labeler - GOJO Industries, Inc. (004162038)
    Registrant - Rockline Industries (966920881)
    Establishment
    NameAddressID/FEIBusiness Operations
    Rockline Idnustries966920881manufacture(21749-359)
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