NDC11 00220094141
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 |
|---|---|
| 00220-0941-41 | 00220-0941 |
| 00220-941-41 | 00220-941 |
| 0220-0941-41 | 0220-0941 |
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 |
|---|---|---|---|---|---|---|
| Bryonia | BRYONIA ALBA ROOT | Boiron | 8489ca49-bfdf-0df7-e053-2991aa0af54f | 2026-01-06 | 0220-0941-41 0220-0941 00220094141 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.