NDC11 59321005602
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 |
|---|---|
| 59321-0056-02 | 59321-0056 |
| 59321-0056-2 | 59321-0056 |
| 59321-056-02 | 59321-056 |
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 |
|---|---|---|---|---|---|---|
| ULTRA STRENGTH ZHENG GU SHUI | MENTHOL AND CAMPHOR | GUANGXI YULIN PHARMACEUTICAL GROUP CO LTD | 53397663-044d-4e48-989b-2c6257af5f84 | 2025-07-14 | Warnings, Adverse reactions | 59321-056-02 59321-056 59321005602 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.