<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
71775-071-52
</NDCCode>
<PackageDescription>
120000 mg in 1 TUBE (71775-071-52)
</PackageDescription>
<NDC11Code>
71775-0071-52
</NDC11Code>
<ProductNDC>
71775-071
</ProductNDC>
<ProductTypeName>
HUMAN OTC DRUG
</ProductTypeName>
<ProprietaryName>
Dinosaur
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Sodium Fluoride
</NonProprietaryName>
<DosageFormName>
PASTE
</DosageFormName>
<RouteName>
DENTAL
</RouteName>
<StartMarketingDate>
20201130
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
OTC MONOGRAPH NOT FINAL
</MarketingCategoryName>
<ApplicationNumber>
part356
</ApplicationNumber>
<LabelerName>
LMZ
</LabelerName>
<SubstanceName>
SODIUM FLUORIDE
</SubstanceName>
<StrengthNumber>
24
</StrengthNumber>
<StrengthUnit>
mg/100mg
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Deprecated
</Status>
<LastUpdate>
2021-01-12
</LastUpdate>
<PackageNdcExcludeFlag>
N
</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>
N
</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>
20211231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>
20201130
</StartMarketingDatePackage>
<EndMarketingDatePackage/>
<SamplePackage>
N
</SamplePackage>
</NDC>