NDC11 59050010701
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 |
|---|---|
| 59050-0107-01 | 59050-0107 |
| 59050-0107-1 | 59050-0107 |
| 59050-107-01 | 59050-107 |
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 |
|---|---|---|---|---|---|---|
| Lightning X POVIDONE IODINE WIPE | POVIDONE IODINE WIPE | Changzhou Maokang Medical Products Co., Ltd. | 04be4c2f-742b-7058-e063-6394a90a460d | 2026-02-25 | Warnings | 59050-107-01 59050-107 59050010701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.