NDC11 49580062406
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 |
|---|---|
| 49580-0624-06 | 49580-0624 |
| 49580-0624-6 | 49580-0624 |
| 49580-624-06 | 49580-624 |
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 |
|---|---|---|---|---|---|---|
| Stomach Relief Regular Strength | BISMUTH SUBSALICYLATE | P & L Development, LLC | 7a461b91-d11f-4cb9-be61-c7d91d278302 | 2024-04-16 | Warnings | 49580-0624-6 49580-0624 49580062406 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.