Label: DISINFECTING WIPES cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated October 18, 2020

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  • DOSAGE & ADMINISTRATION

    Store below 110°F(43°C)

  • INACTIVE INGREDIENT

    AQUA

    PROPYLENE GLYCOL

    PHENOXYETHANOL

    GREEN TEA EXTRACT

    Parfum (Ocean)

  • INDICATIONS & USAGE

    Thoroughly wipe the surface with the product and let it dry. Discardthe wipe properly. Supervise children under six years of age whenusing this product to avoid swallowing.

  • ACTIVE INGREDIENT

    n-Alkyl(68%C12,32%C14) dimethyl ethylbenzyl ammonium chloride

    n-Alkyl(5%C12,60%C14,30%C16,5%C18) dimethyl benzyl ammonium chloride

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • PURPOSE

    Disinfection
    Sterilization
    No Rinseing

  • WARNINGS

    For external use only.When using this product, keep out of eyes,ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    DISINFECTING WIPES 
    disinfecting wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:92763-015
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) (UNII: G258TFN61X) (N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM (C12-C14) - UNII:85440928RV) N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14)1 g  in 50 
    N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) (UNII: 9U1Q4T4ZYS) (BENZALKONIUM - UNII:7N6JUD5X6Y) N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18)1 g  in 50 
    Inactive Ingredients
    Ingredient NameStrength
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    WATER (UNII: 059QF0KO0R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    METHYL BENZOATE (UNII: 6618K1VJ9T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:92763-015-0150 in 1 PACKET; Type 0: Not a Combination Product10/19/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/19/2020
    Labeler - NANOFIXIT VENTURES INC. (723428496)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nanofixit Ventures, Inc.723428496manufacture(92763-015)
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