NDC11 00220019141
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 |
|---|---|
| 00220-0191-41 | 00220-0191 |
| 00220-191-41 | 00220-191 |
| 0220-0191-41 | 0220-0191 |
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 |
|---|---|---|---|---|---|---|
| Aloe | ALOE FEROX LEAF | Boiron | 83ec7cf8-c03b-3cf1-e053-2991aa0a0126 | 2023-06-13 | 0220-0191-41 0220-0191 00220019141 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.