NDC11 00220082041
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 |
|---|---|
| 00220-0820-41 | 00220-0820 |
| 00220-820-41 | 00220-820 |
| 0220-0820-41 | 0220-0820 |
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 |
|---|---|---|---|---|---|---|
| BENZOICUM ACIDUM | BENZOIC ACID | Boiron | 124e1676-96fd-1a52-e063-6294a90a901f | 2024-02-26 | 0220-0820-41 0220-0820 00220082041 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.