{
"NDC": {
"NDCCode": "82910-0602-1",
"PackageDescription": ".085 kg in 1 TUBE (82910-0602-1) ",
"NDC11Code": "82910-0602-01",
"ProductNDC": "82910-0602",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Floraseptic Wound Gel",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Benzethonium Chloride, Allantoin",
"DosageFormName": "GEL",
"RouteName": "TOPICAL",
"StartMarketingDate": "20240630",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH DRUG",
"ApplicationNumber": "M003",
"LabelerName": "BonePharm, LLC",
"SubstanceName": "ALLANTOIN; BENZETHONIUM CHLORIDE",
"StrengthNumber": ".005; .0012",
"StrengthUnit": "kg/kg; kg/kg",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2026-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20251231",
"StartMarketingDatePackage": "20240630",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}