NDC11 30142039805
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 |
|---|---|
| 30142-0398-05 | 30142-0398 |
| 30142-0398-5 | 30142-0398 |
| 30142-398-05 | 30142-398 |
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 |
|---|---|---|---|---|---|---|
| Eye Itch Relief | KETOTIFEN FUMARATE | Kroger Company | eb81286f-72b4-42b3-a596-439d0aeae93f | 2023-12-08 | Warnings | 30142-398-05 30142-398 30142039805 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.