NDC11 11673029108
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 |
|---|---|
| 11673-0291-08 | 11673-0291 |
| 11673-0291-8 | 11673-0291 |
| 11673-291-08 | 11673-291 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 5-Symptom Digestive Relief | BISMUTH SUBSALICYLATE | TARGET CORPORATION | 28fba615-48ca-8d96-e063-6394a90a2797 | 2025-04-12 | Warnings | 11673-291-08 11673-291 11673029108 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.