{
"NDC": {
"NDCCode": "81033-006-01",
"PackageDescription": "100 CUP, UNIT-DOSE in 1 CASE (81033-006-01) / 30 mL in 1 CUP, UNIT-DOSE (81033-006-30) ",
"NDC11Code": "81033-0006-01",
"ProductNDC": "81033-006",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Kesin Mag-al Plus",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Aluminum And Magnesium Hydroxide W/simethicone Suspension",
"DosageFormName": "SUSPENSION",
"RouteName": "ORAL",
"StartMarketingDate": "20251105",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH DRUG",
"ApplicationNumber": "M001",
"LabelerName": "Kesin Pharma Corporation",
"SubstanceName": "ALUMINUM HYDROXIDE; DIMETHICONE, UNSPECIFIED; MAGNESIUM HYDROXIDE",
"StrengthNumber": "200; 20; 200",
"StrengthUnit": "mg/5mL; mg/5mL; mg/5mL",
"Pharm_Classes": "Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Skin Barrier Activity [PE], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2025-11-14",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20251105",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}