<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
81033-042-50
</NDCCode>
<PackageDescription>
50 CUP, UNIT-DOSE in 1 CARTON (81033-042-50) / 30 mL in 1 CUP, UNIT-DOSE (81033-042-30)
</PackageDescription>
<NDC11Code>
81033-0042-50
</NDC11Code>
<ProductNDC>
81033-042
</ProductNDC>
<ProductTypeName>
HUMAN OTC DRUG
</ProductTypeName>
<ProprietaryName>
Mineral Oil
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Mineral Oil
</NonProprietaryName>
<DosageFormName>
SOLUTION
</DosageFormName>
<RouteName>
ORAL
</RouteName>
<StartMarketingDate>
20250301
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
OTC MONOGRAPH DRUG
</MarketingCategoryName>
<ApplicationNumber>
M007
</ApplicationNumber>
<LabelerName>
Kesin Pharma Corporation
</LabelerName>
<SubstanceName>
MINERAL OIL
</SubstanceName>
<StrengthNumber>
1000
</StrengthNumber>
<StrengthUnit>
mg/mL
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Active
</Status>
<LastUpdate>
2025-03-24
</LastUpdate>
<PackageNdcExcludeFlag>
N
</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>
N
</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>
20261231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>
20250301
</StartMarketingDatePackage>
<EndMarketingDatePackage/>
<SamplePackage>
N
</SamplePackage>
</NDC>