NDC11 68007040301
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 |
|---|---|
| 68007-0403-01 | 68007-0403 |
| 68007-0403-1 | 68007-0403 |
| 68007-403-01 | 68007-403 |
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 |
|---|---|---|---|---|---|---|
| Zhuifeng Gao Pain Relieving | MENTHOL | GUILIN CHINA RESOURCES TIANHE PHARMACEUTICAL CO LTD | 3f12da60-26d1-4407-8e02-c3213ea3ad2a | 2025-09-26 | Warnings | 68007-403-01 68007-403 68007040301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.