Label: LAURA GELLER ANTIBACTERIAL HAND SANITIZING WIPES- benzalkonium chloride cloth

  • NDC Code(s): 76635-220-20
  • Packager: Hangzhou Glamcos Biotech CO.,LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 23, 2023

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  • Active Ingredient

    Benzalkonium Chloride 0.2%

  • Purpose

    Antibacterial

  • Use

    For hand sanitization and decreasing amount of bacteria on skin.

  • Warnings

    For External Use Only.
    Do Not Use on children less than 2 years of age.
    On open wounds/cuts.
    When Using This Product keep out of eyes,ears and mouth.In case of contact with eyes,rinse thoroughly with water.
    Stop use and ask a doctor if irritation or rash occurs.These may be signs of a serious condition.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed,get medical help or contact the poison control center immediately.

  • Directions

    Rub cloth between hands for complete cleansing and let hands air dry.
    Children under 6 years of age should be supervised when using.

  • Inactive Ingredients

    Water, Phenoxyethanol, Didecylmdimonium Chloride, Propylene Glycol, Chlophenesin

  • Package Label

    LAURA GELLER antibacterial hand sanitizing wipes-20

  • INGREDIENTS AND APPEARANCE
    LAURA GELLER ANTIBACTERIAL HAND SANITIZING WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76635-220
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Product Characteristics
    Color    Score    
    ShapeSQUARE (20 Piece Cloth) Size
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76635-220-20105 g in 1 BAG; Type 0: Not a Combination Product08/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/11/2020
    Labeler - Hangzhou Glamcos Biotech CO.,LTD (554476017)
    Registrant - Hangzhou Glamcos Biotech CO.,LTD (554476017)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hangzhou Glamcos Biotech CO., LTD554476017manufacture(76635-220)
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