NDC11 67618015005
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 |
|---|---|
| 67618-0150-05 | 67618-0150 |
| 67618-0150-5 | 67618-0150 |
| 67618-150-05 | 67618-150 |
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 |
|---|---|---|---|---|---|---|
| Betadine Solution | POVIDONE-IODINE | Atlantis Consumer Healthcare, Inc. | 1b1e224c-8c00-46ea-9bdd-020a9b45321d | 2026-01-21 | Warnings | 67618-150 |
| Betadine Solution | POVIDONE-IODINE | Atlantis Consumer Healthcare, Inc. | 41891599-420e-48d2-8e31-d28a2209e383 | 2025-01-06 | Warnings | 67618-150-05 67618-150 67618015005 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.