NDC11 69423096612
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 |
|---|---|
| 69423-0966-12 | 69423-0966 |
| 69423-966-12 | 69423-966 |
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 | d800eb8c-42c8-fb12-e053-2a95a90af2a2 | 2026-09-09 | Warnings | 69423-966-12 69423-966 69423096612 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.