NDC11 72459001201
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 |
|---|---|
| 72459-0012-01 | 72459-0012 |
| 72459-0012-1 | 72459-0012 |
| 72459-012-01 | 72459-012 |
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 |
|---|---|---|---|---|---|---|
| OP First Aid Series Povidone Iodine Prep Pad | POVIDONE-IODINE | Yiwu Ori-Power Medtech Co.,Ltd. | b43ae55f-dc21-09b2-e053-2995a90adf4c | 2026-01-01 | Warnings | 72459-012-01 72459-012 72459001201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.