Label: ANTIBACTERIAL- benzalkonium chloride soap

  • NDC Code(s): 41250-976-03, 41250-976-68
  • Packager: Meijer Distribution, INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 21, 2023

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  • Claims

    ANTIBACTERIAL

    hand saop

  • DIRECTIONS:

    Apply to wet hands, lather into rich foam and rinse well.

  • 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

    • if irritation and redness develop
    • comdition 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 throughly
    • rinse thoroughly
  • Inactive ingredients

    water, lauramine oxide, cocamidopropyl betaine, lauramidopropylamine oxide, sodium chloride, myristamidopropylamine oxide, glycerin, fragrance, disteareth-75 IPDI, PEG-150 distearate, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, blue 1, red 33

  • Disclaimer

    *This product is not manufactured or distribute by the Colgate-Palmolive Company, distributor of Softsoap Antibacterial Hand Soap White Tea & Berry.

  • Adverse reaction

    Questions 1-888-593-0593

    DISTRIBUTED BY

    MEIJER DISTRIBUTION, INC

    GRAND RAPIDS, MI 49544

    OUR QUALITY GUARANTEE

    The Meijer Family

    WWW.MEIJER.COM/SATISFACTION

    how2recycle.info

  • Principal Panel Display

    meijer

    ANTIBACTERIAL

    hand soap

    BERRIES & WHITE TEA SCENT

    CONTAINS MOISTURIZERS

    PARABEN FREE & PHTHALATE FREE

    Compare to Softsoap Hand Soap*

    50 FL OZ (1.56 QT) (1.47 L)

    image description

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-976
    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)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DISTEARETH-75 ISOPHORONE DIISOCYANATE (UNII: 5365FJ30SC)  
    PEG-150 distearate (UNII: 6F36Q0I0AC)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41250-976-681656 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/26/2018
    2NDC:41250-976-031478 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/21/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/26/2018
    Labeler - Meijer Distribution, INC (006959555)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(41250-976)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(41250-976)
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