NDC11 50804012101
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 |
|---|---|
| 50804-0121-01 | 50804-0121 |
| 50804-0121-1 | 50804-0121 |
| 50804-121-01 | 50804-121 |
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 |
|---|---|---|---|---|---|---|
| GoodSense Eye Drops Irritation Relief | TETRAHYDROZOLINE HCL, ZINC SULFATE | Geiss, Destin & Dunn, Inc. | 9b24fbdd-780c-1ba2-e053-2a95a90ad60f | 2025-12-30 | Warnings | 50804-121-01 50804-121 50804012101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.