<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
61354-090-02
</NDCCode>
<PackageDescription>
500 mg in 1 TUBE (61354-090-02)
</PackageDescription>
<NDC11Code>
61354-0090-02
</NDC11Code>
<ProductNDC>
61354-090
</ProductNDC>
<ProductTypeName>
HUMAN OTC DRUG
</ProductTypeName>
<ProprietaryName>
Sunscreen
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Zinc Oxide
</NonProprietaryName>
<DosageFormName>
CREAM
</DosageFormName>
<RouteName>
TOPICAL
</RouteName>
<StartMarketingDate>
20210222
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
OTC MONOGRAPH FINAL
</MarketingCategoryName>
<ApplicationNumber>
part352
</ApplicationNumber>
<LabelerName>
Oxygen development
</LabelerName>
<SubstanceName>
ZINC OXIDE
</SubstanceName>
<StrengthNumber>
24
</StrengthNumber>
<StrengthUnit>
mg/100mg
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Deprecated
</Status>
<LastUpdate>
2023-01-03
</LastUpdate>
<PackageNdcExcludeFlag>
N
</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>
N
</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>
20221231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>
20210222
</StartMarketingDatePackage>
<EndMarketingDatePackage/>
<SamplePackage>
N
</SamplePackage>
</NDC>