<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
0363-1500-01
</NDCCode>
<PackageDescription>
1 KIT in 1 CASE (0363-1500-01) * .9 g in 1 POUCH (61010-5600-1) * .34 g in 1 POUCH (51142-445-21) * .9 g in 1 POUCH (61010-5800-1) * 2 TABLET, COATED in 1 PACKET (47682-718-99) * .0019 L in 1 PACKET (61010-2017-0) * 1 TABLET, FILM COATED in 1 PACKET (47682-167-46) * .9 g in 1 PACKET (61010-5701-3)
</PackageDescription>
<NDC11Code>
00363-1500-01
</NDC11Code>
<ProductNDC>
0363-1500
</ProductNDC>
<ProductTypeName>
HUMAN OTC DRUG
</ProductTypeName>
<ProprietaryName>
Walgreens
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Diphenhydramine Hydrochloride, Ibuprofen, Hydrocortisone, Bacitracin Zinc, Neomycin Sulfate, Polymyxin-b Sulfate, Lidocaine Hcl, Benzalkonium Chloride, Isopropyl Alcohol, Ethyl Alcohol
</NonProprietaryName>
<DosageFormName>
KIT
</DosageFormName>
<RouteName>
ORAL
</RouteName>
<StartMarketingDate>
20240717
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
OTC MONOGRAPH DRUG
</MarketingCategoryName>
<ApplicationNumber>
505G(a)(3)
</ApplicationNumber>
<LabelerName>
Walgreen Co.
</LabelerName>
<SubstanceName/>
<StrengthNumber/>
<StrengthUnit/>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Active
</Status>
<LastUpdate>
2026-07-10
</LastUpdate>
<PackageNdcExcludeFlag>
N
</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>
N
</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>
20271231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>
20240717
</StartMarketingDatePackage>
<EndMarketingDatePackage/>
<SamplePackage>
N
</SamplePackage>
</NDC>