NDC11 67777023403
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 |
|---|---|
| 67777-0234-03 | 67777-0234 |
| 67777-0234-3 | 67777-0234 |
| 67777-234-03 | 67777-234 |
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 |
|---|---|---|---|---|---|---|
| Menthol and Zinc Oxide | MENTHOL AND ZINC OXIDE | Dynarex Corporation | d0e43651-4215-465b-9ace-1bc23126b109 | 2024-11-20 | Warnings | 67777-234-03 67777-234 67777023403 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.