Walgreens

Product NDC: 0363-1500
Requested package NDC: 0363-1500-01
11-digit product format: 003631500
Labeler code: 0363
Product ID: 0363-1500_563138ab-2058-29b3-e063-6294a90ab803
Type: HUMAN OTC DRUG
Nonproprietary name: diphenhydramine hydrochloride, ibuprofen, hydrocortisone, bacitracin zinc, neomycin sulfate, polymyxin-B sulfate, lidocaine HCL, benzalkonium chloride, isopropyl alcohol, ethyl alcohol
Dosage form: KIT
Route: ORAL
Labeler: Walgreen Co.
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2024-07-17
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Walgreens
Listing expiration: 2027-12-31

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 7 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
106258	Internal RxNorm lookup
204602	Internal RxNorm lookup
310965	Internal RxNorm lookup
797544	Internal RxNorm lookup
1012100	Internal RxNorm lookup
1039699	Internal RxNorm lookup
1049630	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5630f48b-404c-b847-e063-6394a90a8d8e	Available on FDA.report

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Walgreens	DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN-B SULFATE, LIDOCAINE HCL, BENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL, ETHYL ALCOHOL	Walgreen Co.	5630f48b-404c-b847-e063-6394a90a8d8e	2026-07-09	Warnings	Exact identifier ndc (package): 0363-1500-01 ndc (product): 0363-1500 ndc11 (package): 00363150001

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
0363-1500-01	00363150001	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)	1 kit	2024-07-17	No	No	Current