NDC11 00220082341
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 |
|---|---|
| 00220-0823-41 | 00220-0823 |
| 00220-823-41 | 00220-823 |
| 0220-0823-41 | 0220-0823 |
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 | 6c41ab9f-d45b-fc18-e053-2a91aa0ae235 | 2024-02-27 | 0220-0823-41 0220-0823 00220082341 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.