NDC11 72932001401
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 |
|---|---|
| 72932-0014-01 | 72932-0014 |
| 72932-0014-1 | 72932-0014 |
| 72932-014-01 | 72932-014 |
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 |
|---|---|---|---|---|---|---|
| ZONSEN Roll-On Antiperspirant | ALUMINUM CHLOROHYDRATE | Wuhan Zonsen Medical Products Co., Ltd. | 203375a3-50db-7c1e-e063-6394a90a4039 | 2024-08-21 | Warnings | 72932-014-01 72932-014 72932001401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.