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Zep E-2 Foaming Sanitizing Hand Cleaner (Zep Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 3785 mL in 1 BOTTLE, PLASTIC (66949-994-24) Label Information
LIQUID 2500 mL in 1 BOTTLE, PLASTIC (66949-994-25) Label Information
LIQUID 1000 mL in 1 BOTTLE, PLASTIC (66949-994-01) Label Information
LIQUID 1200 mL in 1 BOTTLE, PLASTIC (66949-994-15) Label Information

Complete Zep E-2 Foaming Sanitizing Hand Cleaner Information

  • Active ingredient

    Chloroxylenol 3.0%


  • Purpose

    Antiseptic Hand Wash


  • Uses

    Hand sanitizing to decrease bacteria on the skin.


  • Warnings

    For external use only.


  • When using this product

    • Avoid eye contact.
    • If in eyes, rinse promptly and thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if skin irritation or redness persists for more than 72 hours.


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children and pets. Children must be supervised in use of this product.


  • ASK DOCTOR

    If swallowed, get medical help or contact a Poison Control center immediately.


  • Directions

    • Wet hands with water.
    • Apply liquid soap.
    • Massage soap into hands and wrists, emphasizing the back of hands, knuckles and cuticles.
    • Rinse hands thoroughly and dry.

  • Other information

    • Store at 20 to 25°C (68 to 77°F).
    • Dispose in accordance with all applicable federal, local and state regulations.

  • Inactive ingredients

    water; sodium C14-16 olefin sulfonate; triethylene glycol; cocamidopropyl betaine; sodium xylenesulfonate; PEG-75 lanolin, citric acid


  • Questions or comments?

    Call 1-800-I-BUY-ZEP (1-800-428-9937)


  • INGREDIENTS AND APPEARANCE
    ZEP E-2 FOAMING SANITIZING HAND CLEANER 
    chloroxylenol liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:66949-994
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 0.3 g  in 10 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    TRIETHYLENE GLYCOL (UNII: 3P5SU53360)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    PEG-75 LANOLIN (UNII: 09179OX7TB)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66949-994-01 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/19/2000
    2 NDC:66949-994-15 1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/19/2000
    3 NDC:66949-994-16 2500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/19/2000
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 06/19/2000
    ZEP E-2 FOAMING SANITIZING HAND CLEANER 
    chloroxylenol liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:66949-271
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 0.3 g  in 10 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    TRIETHYLENE GLYCOL (UNII: 3P5SU53360)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    PEG-75 LANOLIN (UNII: 09179OX7TB)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66949-271-15 1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2011 01/02/2019
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 10/01/2011 01/02/2019
    Labeler - Zep Inc. (030471374)
    Establishment
    Name Address ID/FEI Business Operations
    Zep Inc. 030471374 manufacture(66949-994, 66949-271)