NDC11 50804070001
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 |
|---|---|
| 50804-0700-01 | 50804-0700 |
| 50804-0700-1 | 50804-0700 |
| 50804-700-01 | 50804-700 |
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 |
|---|---|---|---|---|---|---|
| Good Sense Lubricating Plus Lubricant Eye Drops | CARBOXYMETHYLCELLULOSE SODIUM | GoodSense | ffd6428e-3bf5-8742-e053-6394a90a4c8f | 2025-12-30 | Warnings | 50804-700-01 50804-700 50804070001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.