{
"NDC": {
"NDCCode": "50066-001-01",
"PackageDescription": "1 TUBE in 1 BOX (50066-001-01) > 25 g in 1 TUBE",
"NDC11Code": "50066-0001-01",
"ProductNDC": "50066-001",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Nikzon",
"ProprietaryNameSuffix": "Hemorrhoidal",
"NonProprietaryName": "Phenylephrine Hydrochloride And Pramoxine Hydrochloride",
"DosageFormName": "CREAM",
"RouteName": "TOPICAL",
"StartMarketingDate": "20131201",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH FINAL",
"ApplicationNumber": "part346",
"LabelerName": "Genoma Lab USA Inc",
"SubstanceName": "PHENYLEPHRINE HYDROCHLORIDE; PRAMOXINE HYDROCHLORIDE",
"StrengthNumber": "2.5; 10",
"StrengthUnit": "mg/g; mg/g",
"Pharm_Classes": "Adrenergic alpha1-Agonists [MoA], alpha-1 Adrenergic Agonist [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20241231",
"StartMarketingDatePackage": "20190619",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}