NDC11 21130012540
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 |
|---|---|
| 21130-0125-40 | 21130-0125 |
| 21130-125-40 | 21130-125 |
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 | BISMUTH SUBSALICYLATE | SAFEWAY | 5538d56a-b258-4260-b51b-f5131bd76885 | 2025-10-29 | Warnings | 21130-125-40 21130-125 21130012540 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.