{
"NDC": {
"NDCCode": "10157-2127-1",
"PackageDescription": "1 TUBE in 1 CARTON (10157-2127-1) / 11.9 g in 1 TUBE",
"NDC11Code": "10157-2127-01",
"ProductNDC": "10157-2127",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Kanka Triple Action",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Benzocaine And Menthol, Unspecified Form",
"DosageFormName": "GEL",
"RouteName": "ORAL",
"StartMarketingDate": "20250106",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH DRUG",
"ApplicationNumber": "M022",
"LabelerName": "Blistex Inc.",
"SubstanceName": "BENZOCAINE; MENTHOL, UNSPECIFIED FORM",
"StrengthNumber": "20; 2",
"StrengthUnit": "g/100g; g/100g",
"Pharm_Classes": "Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2025-01-14",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20250106",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}