NDC11 00363130202

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
00363-1302-02	00363-1302
00363-1302-2	00363-1302
0363-1302-02	0363-1302

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
Ultra Strength digestive relief	BISMUTH SUBSALICYLATE	WALGREENS CO.	756e7a47-7e14-4694-84fa-ca6396f7edcc	2025-11-26	Warnings	Exact identifier ndc (package): 0363-1302-02 ndc (product): 0363-1302 ndc11 (package): 00363130202

Reported adverse events (FAERS/openFDA)#

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