NDC11 55614070001
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 |
|---|---|
| 55614-0700-01 | 55614-0700 |
| 55614-0700-1 | 55614-0700 |
| 55614-700-01 | 55614-700 |
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 |
|---|---|---|---|---|---|---|
| WU YANG BRAND PAIN RELIEVING MEDICATED | MENTHOL AND CAMPHOR | MADISON ONE ACME INC | 05c6b95a-aeb6-4234-97c7-8d77eccb38d8 | 2025-11-10 | Warnings | 55614-700-01 55614-700 55614070001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.