NDC11 37000044012
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 |
|---|---|
| 37000-0440-12 | 37000-0440 |
| 37000-440-12 | 37000-440 |
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 |
|---|---|---|---|---|---|---|
| Pepto-Bismol Ultra | BISMUTH SUBSALICYLATE | The Procter & Gamble Manufacturing Company | 673893bd-f8e9-23b0-e053-2a91aa0aa1d4 | 2026-03-12 | Warnings | 37000-440-12 37000-440 37000044012 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.