NDC11 11673072416
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 |
|---|---|
| 11673-0724-16 | 11673-0724 |
| 11673-724-16 | 11673-724 |
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 |
|---|---|---|---|---|---|---|
| Digestive Relief Regular Strength | BISMUTH SUBSALICYLATE | TARGET Corporation | e8107300-921c-4ba4-ad6e-f4cf1cd5c295 | 2026-08-20 | Warnings | 11673-724-16 11673-724 11673072416 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.