{
"NDC": {
"NDCCode": "43742-0240-1",
"PackageDescription": "30 mL in 1 BOTTLE, SPRAY (43742-0240-1) ",
"NDC11Code": "43742-0240-01",
"ProductNDC": "43742-0240",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Radiation",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Chondrus Crispus, Fucus Vesiculosus, Thyroidinum (suis), Cadmium Iodatum, Iodium, Strontium Carbonicum, X-ray,",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20121213",
"EndMarketingDate": "20251213",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"ApplicationNumber": null,
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "ALCOHOL, X-RAY EXPOSED (1000 RAD); CADMIUM IODIDE; CHONDRUS CRISPUS; FUCUS VESICULOSUS; IODINE; RADIUM BROMIDE; STRONTIUM CARBONATE; THYROID",
"StrengthNumber": "30; 12; 3; 3; 12; 33; 12; 8",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-12-16",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20121213",
"EndMarketingDatePackage": "20251213",
"SamplePackage": "N"
}
}