NDC11 84520002304
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 |
|---|---|
| 84520-0023-04 | 84520-0023 |
| 84520-0023-4 | 84520-0023 |
| 84520-023-04 | 84520-023 |
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 |
|---|---|---|---|---|---|---|
| Lume Soft Powder | ALUMINUM CHLOROHYDRATE | Lume Deodorant, LLC. | 47be0eea-097f-4030-e063-6294a90ad48c | 2026-02-09 | Warnings | 84520-023-04 84520-023 84520002304 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.