<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
71630-176-18
</NDCCode>
<PackageDescription>
170 g in 1 BOTTLE, SPRAY (71630-176-18)
</PackageDescription>
<NDC11Code>
71630-0176-18
</NDC11Code>
<ProductNDC>
71630-176
</ProductNDC>
<ProductTypeName>
HUMAN OTC DRUG
</ProductTypeName>
<ProprietaryName>
Doterra Sun Body
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Mineral Sunscreen
</NonProprietaryName>
<DosageFormName>
SPRAY
</DosageFormName>
<RouteName>
TOPICAL
</RouteName>
<StartMarketingDate>
20260812
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
OTC MONOGRAPH DRUG
</MarketingCategoryName>
<ApplicationNumber>
M020
</ApplicationNumber>
<LabelerName>
doTERRA International, LLC
</LabelerName>
<SubstanceName>
ZINC OXIDE
</SubstanceName>
<StrengthNumber>
16.8
</StrengthNumber>
<StrengthUnit>
g/100g
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Active
</Status>
<LastUpdate>
2026-08-13
</LastUpdate>
<PackageNdcExcludeFlag>
N
</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>
N
</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>
20271231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>
20260812
</StartMarketingDatePackage>
<EndMarketingDatePackage/>
<SamplePackage>
N
</SamplePackage>
</NDC>