NDC11 71105010505
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 |
|---|---|
| 71105-0105-05 | 71105-0105 |
| 71105-0105-5 | 71105-0105 |
| 71105-105-05 | 71105-105 |
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 |
|---|---|---|---|---|---|---|
| Lubricant Eye Drops | CARBOXYMETHYLCELLULOSE SODIUM | Redicare LLC | 4d1e5089-22b0-7b3f-e063-6294a90a346a | 2026-03-16 | Warnings | 71105-105-05 71105-105 71105010505 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.