{
"NDC": {
"NDCCode": "48951-3267-8",
"PackageDescription": "120 g in 1 TUBE, WITH APPLICATOR (48951-3267-8) ",
"NDC11Code": "48951-3267-08",
"ProductNDC": "48951-3267",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Calendula Thuja",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Calendula Thuja",
"DosageFormName": "GEL",
"RouteName": "TOPICAL",
"StartMarketingDate": "20090901",
"EndMarketingDate": null,
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"ApplicationNumber": null,
"LabelerName": "Uriel Pharmacy Inc.",
"SubstanceName": "CALENDULA OFFICINALIS FLOWERING TOP; CANDIDA ALBICANS; ECHINACEA, UNSPECIFIED; LILIUM LANCIFOLIUM WHOLE FLOWERING; ORIGANUM MAJORANA WHOLE; PULSATILLA VULGARIS; SILVER; THUJA OCCIDENTALIS WHOLE; WOOD CREOSOTE",
"StrengthNumber": "2; 30; 2; 3; 2; 6; 7; 3; 6",
"StrengthUnit": "[hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g",
"Pharm_Classes": "Allergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2026-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20251231",
"StartMarketingDatePackage": "20090901",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}