Label: EVERWIPE ANTIBACTERIAL- benzalkonium chloride liquid

  • NDC Code(s): 50157-264-43
  • Packager: Brands International Corporation
  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated April 16, 2021

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  • ACTIVE INGREDIENT

    Benzalkonium Chloride - 0.13%

  • PURPOSE

    Purpose: Antibacterial

  • INDICATIONS & USAGE

    Effective in destroying bacteria to provide antiseptic cleaning.

  • DOSAGE & ADMINISTRATION

    Direction

    • wet hands
    • apply palmful to hands
    • scrub thoroughly
    • rinse
  • WARNINGS

    For external use only

  • STOP USE

    Stop use and ask a doctor if irritation or redness develops

  • WHEN USING

    When using this product

    • do not get it into eyes. If contact occurs, rinse eye thoroughly with water
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

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

  • INACTIVE INGREDIENT

    Lauramidopropylamine oxide, Lauryl glucoside, PEG-150 distearate, Glycol Stearate, Perfume, Aloe extract, Tocopheryl Acetate, Peg 7- Glyceryl Cocoate, Cetrimonium, Chloride, Citric Acid, Glycerin, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone.

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    EVERWIPE ANTIBACTERIAL 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50157-264
    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
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DITETRACYCLINE TETRASODIUM EDETATE (UNII: WX0A0IT7K5)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
    PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50157-264-43443 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/26/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/16/2021
    Labeler - Brands International Corporation (243748238)
    Registrant - Brands International Corporation (243748238)
    Establishment
    NameAddressID/FEIBusiness Operations
    Brands International Corporation243748238manufacture(50157-264)
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