NDC11 69729061201
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 |
|---|---|
| 69729-0612-01 | 69729-0612 |
| 69729-0612-1 | 69729-0612 |
| 69729-612-01 | 69729-612 |
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 |
|---|---|---|---|---|---|---|
| VAGISTEN-V 7 DAY | MICONAZOLE NITRATE | OPMX LLC | a5bfa501-5ae1-4434-bc31-995d0665b99e | 2024-09-04 | Warnings | 69729-612-01 69729-612 69729061201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.