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Zep Professional E-2 Hand Cleaner (Zep Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 3785 mL in 1 BOTTLE, PLASTIC (66949-112-24) Label Information
LIQUID 1000 mL in 1 BOTTLE, PLASTIC (66949-112-01) Label Information

Complete Zep Professional E-2 Hand Cleaner Information

  • 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


  • INGREDIENTS AND APPEARANCE
    ZEP PROFESSIONAL E-2 HAND CLEANER 
    benzalkonium chloride liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:66949-112
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE .013 g  in 10 mL
    Inactive Ingredients
    Ingredient Name Strength
    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 Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66949-112-01 1000 mL in 1 BOTTLE, PLASTIC
    2 NDC:66949-112-24 3785 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 04/07/2009
    Labeler - Zep Inc. (030471374)
    Establishment
    Name Address ID/FEI Business Operations
    Zep Inc. 030471374 manufacture(66949-112)