Label: ZEP E-2 HAND SANITIZING CLEANER- chloroxylenol liquid

  • NDC Code(s): 66949-125-01, 66949-125-06, 66949-125-24
  • Packager: Zep Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 20, 2023

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  • Active ingredient

    Chloroxylenol 3.0%

  • Purpose

    Antiseptic Hand Wash

  • Uses

    Hand washing to decrease bacteria on skin

  • Warnings

    For external use only.

  • Do not use

    Do not use in or around the eyes.

  • When using this product

    • If eye contact occurs, rinse promptly and thoroughly with water.
    • Do not swallow.
    • If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.
    • Allergy alert: May cause skin reactions. Symptoms may include: skin reddening, blisters, rash
    • If a skin reaction occurs, stop use and seek medical help right away
  • Stop use and ask a doctor

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

  • Keep out of reach of children and pets

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

  • Directions

    • Wet hands with water.
    • Place hands under dispenser and apply liquid soap.
    • Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles.
    • Rinse hands thoroughly and dry.
  • Other information

    • Store at room temperature.
    • Do not freeze.
    • Dispose in accordance with all applicable federal, state and local regulations.
  • Inactive ingredients

    Water, Sodium C14-16 Olefin Sulfonate, Triethylene Glycol, Cocamidopropyl Hydroxysultaine, Hydroxyethyl Cellulose, PEG-75 Lanolin, Methylchloroisothiazolinone, Methylisothiazolinone, Citric Acid

  • Questions of comments?

    Call 1-877-I-BUY_ZEP (1-877-428-9937)

  • PRINCIPAL DISPLAY PANEL

    125_0920

  • INGREDIENTS AND APPEARANCE
    ZEP E-2 HAND SANITIZING CLEANER 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-125
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    TRIETHYLENE GLYCOL (UNII: 3P5SU53360)  
    COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
    HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)  
    PEG-75 LANOLIN (UNII: 09179OX7TB)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-125-2415140 mL in 1 CASE; Type 0: Not a Combination Product06/15/1988
    2NDC:66949-125-0111400 mL in 1 CASE; Type 0: Not a Combination Product06/15/1988
    3NDC:66949-125-066000 mL in 1 CASE; Type 0: Not a Combination Product06/15/198812/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/15/1988
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.112125310manufacture(66949-125)
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