Label: ZEP HANDSTAND ANTIMICROBIAL- benzalkonium chloride liquid

  • 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

    Antibacterial handwashing

  • Uses

    Handwash to help decrease bacteria on the skin.

  • Warnings

    For external use only.

  • Do not use

    Do not use in the eyes. In case of eye contact, immediately flush with water.

  • Stop use and ask a doctor

    Stop use and ask a doctor if irritation or rash appears and lasts.

  • Keep out of reach of children

    Keep out of reach of children. If swallow, get medical help or contact a Poison Control Center right away.

  • Directions

    • Apply a small amount, covering hands with product for 30 seconds. Add water, lather and rinse.
    • Children under 6 years of age should be supervised when using this product.
  • Inactive Ingredients

    Water, Cetrimonium Chloride, Sodium Chloride, Lauramine Oxide, Sorbitol, Disodium EDTA, Cocamide MEA, PEG-120 Methyl Glucose Dioleate, Sodium Lauriminodipropionate, Citric Acid, Fragrance, Methylisothiazolinone, Methylchloroisothiazolinone, Yellow 5, Red 33

  • QUESTIONS

    1-877-I-BUY-ZEP/1-877-428-9937

  • PRINCIPAL DISPLAY PANEL

    127_U429

  • INGREDIENTS AND APPEARANCE
    ZEP HANDSTAND ANTIMICROBIAL 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-127
    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
    SODIUM LAURIMINODIPROPIONATE (UNII: 7G447D0DH9)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    SORBITOL (UNII: 506T60A25R)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    WATER (UNII: 059QF0KO0R)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-127-019600 mL in 1 CASE; Type 0: Not a Combination Product08/23/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/23/2017
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kutol Products Company004236139manufacture(66949-127)
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