NDC11 61333020301
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 |
|---|---|
| 61333-0203-01 | 61333-0203 |
| 61333-0203-1 | 61333-0203 |
| 61333-203-01 | 61333-203 |
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 |
|---|---|---|---|---|---|---|
| Lights Povidone Iodine Prep Pad | POVIDONE-IODINE | Lights Medical Manufacture Co., Ltd. | e561332d-e419-43db-a68e-0c0d49b01c9a | 2026-01-21 | Warnings | 61333-203-01 61333-203 61333020301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.