NDC11 10565006702
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 |
|---|---|
| 10565-0067-02 | 10565-0067 |
| 10565-0067-2 | 10565-0067 |
| 10565-067-02 | 10565-067 |
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 |
|---|---|---|---|---|---|---|
| Anti-Perspirant Deodorant | ALUMINUM CHLOROHYDRATE | Hydrox Laboratories | 685b948a-3b22-40ef-9df8-01b3c7757314 | 2026-01-12 | Warnings | 10565-067-02 10565-067 10565006702 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.