{
"NDC": {
"NDCCode": "72042-003-03",
"PackageDescription": "1 TUBE in 1 CARTON (72042-003-03) > 28300 mg in 1 TUBE",
"NDC11Code": "72042-0003-03",
"ProductNDC": "72042-003",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Burn Relief",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Allantoin, Lidocaine, Menthol",
"DosageFormName": "CREAM",
"RouteName": "TOPICAL",
"StartMarketingDate": "20180516",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
"ApplicationNumber": "part348",
"LabelerName": "HUMN Pharmaceuticals Inc",
"SubstanceName": "ALLANTOIN; LIDOCAINE HYDROCHLORIDE ANHYDROUS; MENTHOL",
"StrengthNumber": "1.5; 4; 1",
"StrengthUnit": "mg/100mg; mg/100mg; mg/100mg",
"Pharm_Classes": "Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2024-01-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20231231",
"StartMarketingDatePackage": "20180519",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}