NDC11 30142013824
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 |
|---|---|
| 30142-0138-24 | 30142-0138 |
| 30142-138-24 | 30142-138 |
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 |
|---|---|---|---|---|---|---|
| Ultra Strength digestive relief | BISMUTH SUBSALICYLATE | THE KROGER CO. | 5e288108-1578-4379-a3d6-44b447187643 | 2026-09-01 | Warnings | 30142-138-24 30142-138 30142013824 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.