NDC11 83807001201
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 |
|---|---|
| 83807-0012-01 | 83807-0012 |
| 83807-0012-1 | 83807-0012 |
| 83807-012-01 | 83807-012 |
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 |
|---|---|---|---|---|---|---|
| EVERLIT CARE PRODUCTS IODINE PREP PAD | POVIDONE-IODINE | EVERLIT GLOBAL INC. | 5cbdb73d-333a-4244-a1c0-be430632f0ed | 2026-02-09 | Warnings | 83807-012-01 83807-012 83807001201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.