NDC11 71573012112
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 |
|---|---|
| 71573-0121-12 | 71573-0121 |
| 71573-121-12 | 71573-121 |
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 |
|---|---|---|---|---|---|---|
| Prosoria Medicated | SELENIUM SULFIDE | Nuvothera, Inc. | 44eaaeb0-1400-4697-85d0-e8c2282c1cba | 2024-01-11 | Warnings | 71573-121-12 71573-121 71573012112 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.