NDC11 00363007308
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 |
|---|---|
| 00363-0073-08 | 00363-0073 |
| 00363-0073-8 | 00363-0073 |
| 00363-073-08 | 00363-073 |
| 0363-0073-08 | 0363-0073 |
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 |
|---|---|---|---|---|---|---|
| Soothe | BISMUTH SUBSALICYLATE | Walgreens | a2b2b0ce-034e-4857-bfca-0087bb31878e | 2024-07-25 | Warnings | 0363-0073-08 0363-0073 00363007308 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.