Label: ANTIBACTERIAL HAND WHITE TEA AND EUCALYPTUS- benzalkonium chloride soap

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

Drug Label Information

Updated March 9, 2024

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  • Active Ingredient

    Benzalkonium chloride 0.13%

  • Purpose

    Antibacterial

  • Use

    for handwashing to decrease bacteria on the skin

  • Warnings

    For external use only: hands only

  • When using this product

    • avoid contact with eyes. If contact occurs, rinse eyes with water.
  • Stop use and ask a doctor if 

    • irritation and redness develop
    • condition persists for more than 72 hours
  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    ■ wet hands ■ apply palmful to hands ■ scrub thoroughly ■ rinse thoroughly

  • Inactive Ingredients 

    water, lauramine oxide, cocamidopropyl betaine, lauramidopropylamine oxide, glycerin, myristamidopropylamine oxide, fragrance, linalool, disteareth-75 IPDI, PEG-150 distearate, citric acid, sodium chloride, tetrasodium EDTA, benzophenone-4, sodium benzoate, ext. violet 2

  • Adverse reaction

    Distributed by: Vi-Jon, LLC, St. Louis, MO 63114

    FORMULA MADE IN USA

    EMPLOYEE-OWNED

  • Principal Panel Display

    germ-x

    ANTIBACTERIAL

    LIQUID HAND SOAP

    WHITE TEA & EUCALYPTUS SCENT

    Dermatologist Tested

    12FL OZ (355 ML)

    image description

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL HAND WHITE TEA AND EUCALYPTUS 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83986-140
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    DISTEARETH-75 ISOPHORONE DIISOCYANATE (UNII: 5365FJ30SC)  
    PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83986-140-32355 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/12/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/12/2022
    Labeler - UpLift Brands LLC (119091527)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(83986-140)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(83986-140)
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