ZEP PROFESSIONAL E-2 HAND CLEANER (BENZALKONIUM CHLORIDE) LIQUID [ZEP INC.]

ZEP PROFESSIONAL E-2 HAND CLEANER (BENZALKONIUM CHLORIDE) LIQUID [ZEP INC.]
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NDC 66949-112-01, 66949-112-24
Set ID 0aea9e77-4fb0-417f-86a8-ed8678132621
Category HUMAN OTC DRUG LABEL
Packager Zep Inc.
Generic Name
Product Class
Product Number
Application Number PART333A
  • Active ingredient

    Benzalkonium chloride 0.13%

  • Purpose

    Antiseptic Handwash

  • Uses

    • Hand sanitizing to decrease bacteria on skin
    • For use in food processing facilities
  • Warnings

    For external use only.

  • DO NOT USE

    Can cause eye irritation. Avoid contact with eyes.

  • WHEN USING

    When using this product

    • Do not use in or around eyes. If eye contact occurs, rinse well with water for at least 15 minutes. Consult a physician.
    • Do no swallow this product. If swallowed, do not induce vomiting. If individual is conscious, give large quantities of water to drink and consult a physician immediately.
  • STOP USE

    Discontinue use if irritation and redness develops. If condition persists for more than 72 hours, consult a doctor.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • Directions

    • Wet hands with water
    • Dispense one or two squirts in palm of hand
    • Massag soap into hands and wrists, emphasizing back of hands, knuckles and cuticles
    • Hands must be thoroughly rinsed with potable water
  • Other information

    • Keep container closed
    • Store at room temperature
    • Do not freeze
    • Do not reuse empty container
    • Dispose in accordance with all applicable federal, state & local regulations
  • Inactive ingredients

    Water, Cocamidopropyl Betaine, Didecyldimethylammonium Chloride, PEG-6 Cocamide, Ethanol, Hydroxyethylcellusolose, DMDM Hydantoin (and) Iodopropynyl Butylcarbamate, Citric Acid

  • PRINCIPAL DISPLAY PANEL

    r112.jpg

  • INGREDIENTS AND APPEARANCE
    ZEP PROFESSIONAL E-2 HAND CLEANER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-112
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE.013 g  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    DIDECYLDIMETHYLAMMONIUM CHLORIDE (UNII: JXN40O9Y9B)  
    PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)  
    ALCOHOL (UNII: 3K9958V90M)  
    HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    GLUTARAL (UNII: T3C89M417N)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-112-011000 mL in 1 BOTTLE, PLASTIC
    2NDC:66949-112-243785 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/07/2009
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.030471374manufacture(66949-112)

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