{
"NDC": {
"NDCCode": "12745-177-03",
"PackageDescription": "3785 mL in 1 BOTTLE, PLASTIC (12745-177-03) ",
"NDC11Code": "12745-0177-03",
"ProductNDC": "12745-177",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Medi Fect",
"ProprietaryNameSuffix": "Antiseptic Hand Wash",
"NonProprietaryName": "Ethyl Alcohol",
"DosageFormName": "LIQUID",
"RouteName": "TOPICAL",
"StartMarketingDate": "20010514",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH DRUG",
"ApplicationNumber": "M003",
"LabelerName": "Medical Chemical Corporation",
"SubstanceName": "ALCOHOL; DIAZOLIDINYL UREA",
"StrengthNumber": "59.86; 1",
"StrengthUnit": "g/100mL; g/100mL",
"Pharm_Classes": "Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2025-08-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20010514",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}