NDC11 34666029101
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 |
|---|---|
| 34666-0291-01 | 34666-0291 |
| 34666-0291-1 | 34666-0291 |
| 34666-291-01 | 34666-291 |
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 |
|---|---|---|---|---|---|---|
| Hemorrhoid-X Treatment Pack | HEMORRHOID-X TREATMENT PACK | Nartex Laboratorios Homeopaticos SA DE CV | 8657c12e-5a09-1fcb-e053-2a91aa0aa144 | 2019-04-12 | Warnings | 34666-291-01 34666-291 34666029101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.