NDC11 47682019383
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 |
|---|---|
| 47682-0193-83 | 47682-0193 |
| 47682-193-83 | 47682-193 |
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 |
|---|---|---|---|---|---|---|
| Medi-First Lubricant Eye Drops | CARBOXYMETHYLCELLULOSE SODIUM | Unifirst First Aid Corporation | a4e651cc-adf0-af9e-e053-2995a90ace5a | 2025-12-30 | Warnings | 47682-193-83 47682-193 47682019383 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.