Label: XENODINE- iodine solution

  • NDC Code(s): 86075-001-08, 86075-001-12
  • Packager: Bipore Inc
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated December 29, 2016

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  • Actives

    Iodine 1 %

  • Inactives

    polypropylene glycol and polyethylene glycol

  • Product Labels

    8 fl oz12 fl oz

  • INGREDIENTS AND APPEARANCE
    XENODINE 
    iodine solution
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:86075-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ETHYLENE GLYCOL (UNII: FC72KVT52F)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:86075-001-08237 mL in 1 BOTTLE
    2NDC:86075-001-12355 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/30/2016
    Labeler - Bipore Inc (176929750)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bipore Inc176929750manufacture
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Safety

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Clinical Trials, PubMed, Biochemical Data Summary

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