NDC11 84167042301
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 |
|---|---|
| 84167-0423-01 | 84167-0423 |
| 84167-0423-1 | 84167-0423 |
| 84167-423-01 | 84167-423 |
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 |
|---|---|---|---|---|---|---|
| APUREE Nailtific Extra-Max Strength Daytime Antigungal | APUREE NAILTIFIC EXTRA-MAX STRENGTH DAYTIME ANTIGUNGAL | Guangzhou Meixi Biotechnology Co., Ltd. | 4e3d226b-57f1-75a6-e063-6394a90a96cd | 2026-03-30 | Warnings | 84167-423-01 84167-423 84167042301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.