NDC11 00220094941
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 |
|---|---|
| 00220-0949-41 | 00220-0949 |
| 00220-949-41 | 00220-949 |
| 0220-0949-41 | 0220-0949 |
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 | 8502ac84-1022-e92d-e053-2991aa0a38bc | 2026-01-05 | 0220-0949-41 0220-0949 00220094941 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.