<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
62169-203-12
</NDCCode>
<PackageDescription>
12 BOTTLE, PLASTIC in 1 PACKAGE (62169-203-12) / 500 mL in 1 BOTTLE, PLASTIC (62169-203-17)
</PackageDescription>
<NDC11Code>
62169-0203-12
</NDC11Code>
<ProductNDC>
62169-203
</ProductNDC>
<ProductTypeName>
HUMAN OTC DRUG
</ProductTypeName>
<ProprietaryName>
Aniosgel 85
</ProprietaryName>
<ProprietaryNameSuffix>
Npc
</ProprietaryNameSuffix>
<NonProprietaryName>
Ethanol
</NonProprietaryName>
<DosageFormName>
GEL
</DosageFormName>
<RouteName>
TOPICAL
</RouteName>
<StartMarketingDate>
20140401
</StartMarketingDate>
<EndMarketingDate>
20270831
</EndMarketingDate>
<MarketingCategoryName>
OTC MONOGRAPH DRUG
</MarketingCategoryName>
<ApplicationNumber>
505G(a)(3)
</ApplicationNumber>
<LabelerName>
Laboratoires Anios
</LabelerName>
<SubstanceName>
ALCOHOL
</SubstanceName>
<StrengthNumber>
377.5
</StrengthNumber>
<StrengthUnit>
mL/500mL
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Active
</Status>
<LastUpdate>
2025-02-13
</LastUpdate>
<PackageNdcExcludeFlag>
N
</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>
N
</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough/>
<StartMarketingDatePackage>
20180307
</StartMarketingDatePackage>
<EndMarketingDatePackage>
20270831
</EndMarketingDatePackage>
<SamplePackage>
N
</SamplePackage>
</NDC>