Label: ZEP FS ANTIMICROBIAL HAND CLEANER- benzalkonium chloride liquid

  • NDC Code(s): 66949-105-01, 66949-105-11, 66949-105-24, 66949-105-85
  • Packager: Zep Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 18, 2024

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  • Active ingredient

    Benzalkonium chloride 0.13%

  • Purpose

    Antiseptic Hand Wash

  • Uses

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

    For external use only.

    Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water.

  • When using this product

    • 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.
  • 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 20 to 25°C (68 to 77°F).
    • Do not freeze.
    • Dispose in accordance with all applicable federal, state and local regulations.
  • Inactive ingredients

    Water, Didecyldimonium Chloride, Cocamidopropyl Hydroxysultaine, Lauramine Oxide, PEG-6 Cocamide, Hydroxyethylcellulose, Methylchloroisothiazolinone and Methylisothiazolinone, Citric Acid

  • Questions or comments?

    Call 1-877-I-BUY-ZEP (1-877-428-9937)

  • PRINCIPAL DISPLAY PANEL

    105_3153

  • INGREDIENTS AND APPEARANCE
    ZEP FS ANTIMICROBIAL HAND CLEANER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-105
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-105-0111400 mL in 1 CASE; Type 0: Not a Combination Product06/01/2020
    2NDC:66949-105-116000 mL in 1 CASE; Type 0: Not a Combination Product06/01/2020
    3NDC:66949-105-2415140 mL in 1 CASE; Type 0: Not a Combination Product06/01/2020
    4NDC:66949-105-85208198 mL in 1 DRUM; Type 0: Not a Combination Product06/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/01/2020
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.112125310manufacture(66949-105)
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