NDC11 42913002501
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 |
|---|---|
| 42913-0025-01 | 42913-0025 |
| 42913-0025-1 | 42913-0025 |
| 42913-025-01 | 42913-025 |
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 |
|---|---|---|---|---|---|---|
| Power Stick for Her Powder Fresh | ALUMINUM SESQUICHLOROHYDRATE | A.P. Deauville, LLC | e9696499-e559-47eb-b3c2-b14e80724554 | 2026-04-29 | Warnings | 42913-025-01 42913-025 42913002501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.