Label: ZEP ANTIBACTERIAL HS- benzalkonium chloride liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 20, 2023

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  • Active ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antiseptic Handwash

  • Uses

    Hand washing to decrease bacteria on skin.

  • Warnings

    For external use only.

  • Do not use

    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

    Keep out of reach of children except under adult supervision.

  • 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 thoroughly.
  • Other Information

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

    Water, Cetrimonium Chloride, Lauryl/Myristyl Amidopropyl Amine Oxide, Glycerin, Cocamide DIPA, PEG-120 Methyl Glucose Dioleate, Sodium Chloride, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Tetrasodium EDTA, Fragrance, Yellow 5, Red 4

  • Questions or comments?

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

  • PRINCIPAL DISPLAY PANEL

    110_R461

  • INGREDIENTS AND APPEARANCE
    ZEP ANTIBACTERIAL HS 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-110
    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
    LAUROYL/MYRISTOYL AMIDOPROPYL AMINE OXIDE (UNII: HY9O6ZW9CY)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-110-166000 mL in 1 CASE; Type 0: Not a Combination Product06/29/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/29/2020
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.112125310manufacture(66949-110)
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