{
"NDC": {
"NDCCode": "64471-196-48",
"PackageDescription": "7200 mg in 1 BLISTER PACK (64471-196-48) ",
"NDC11Code": "64471-0196-48",
"ProductNDC": "64471-196",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Allercetin",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Euphrasia Officinalis, Kali Iodatum, Sabadilla, Sticta Pulmonaria, Histaminum Hydrochloricum, Quercetin, Succinicum Acidum, Ambrosia Artemisiaefolia",
"DosageFormName": "TABLET, CHEWABLE",
"RouteName": "ORAL",
"StartMarketingDate": "20140905",
"EndMarketingDate": null,
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"ApplicationNumber": null,
"LabelerName": "Source Naturals, Inc.",
"SubstanceName": "AMBROSIA ARTEMISIIFOLIA WHOLE; EUPHRASIA STRICTA; HISTAMINE DIHYDROCHLORIDE; LOBARIA PULMONARIA; POTASSIUM IODIDE; QUERCETIN; SCHOENOCAULON OFFICINALE SEED; SUCCINIC ACID",
"StrengthNumber": "30; 6; 12; 6; 6; 12; 6; 12",
"StrengthUnit": "[hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg; [hp_X]/mg",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2024-11-06",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20140905",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}