{
"NDC": {
"NDCCode": "51531-0813-1",
"PackageDescription": "1 TUBE in 1 CARTON (51531-0813-1) > 28 g in 1 TUBE",
"NDC11Code": "51531-0813-01",
"ProductNDC": "51531-0813",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Mary Kay Acne Treatment",
"ProprietaryNameSuffix": "Acne Medication",
"NonProprietaryName": "Benzoyl Peroxide",
"DosageFormName": "GEL",
"RouteName": "TOPICAL",
"StartMarketingDate": "19880119",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH FINAL",
"ApplicationNumber": "part333D",
"LabelerName": "Mary Kay Inc.",
"SubstanceName": "BENZOYL PEROXIDE",
"StrengthNumber": "5",
"StrengthUnit": "g/100g",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2017-11-15",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}