NDC11 00220067541
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 |
|---|---|
| 00220-0675-41 | 00220-0675 |
| 00220-675-41 | 00220-675 |
| 0220-0675-41 | 0220-0675 |
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 |
|---|---|---|---|---|---|---|
| Aurum muriaticum | GOLD TRICHLORIDE | Boiron | 8462d926-7aba-58bb-e053-2991aa0ad0dc | 2023-11-08 | 0220-0675-41 0220-0675 00220067541 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.