NDC11 69876174000
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 |
|---|---|
| 69876-1740-0 | 69876-1740 |
| 69876-1740-00 | 69876-1740 |
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 |
|---|---|---|---|---|---|---|
| NEUROFLEX Topical Pain Relieving Liquid | CAMPHOR (SYNTHETIC), MENTHOL | Almark Products Inc | 6da3aa84-7a01-4041-8792-a4bbf49e6e4e | 2023-11-10 | Warnings | 69876-1740-0 69876-1740 69876174000 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.