NDC11 87817010101
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 |
|---|---|
| 87817-0101-01 | 87817-0101 |
| 87817-0101-1 | 87817-0101 |
| 87817-101-01 | 87817-101 |
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 |
|---|---|---|---|---|---|---|
| PureWellness FUNGAL FUSION Antifungal and Antimicrobial Kit | FUNGAL FUSION ANTIFUNGAL AND ANTIMICROBIAL KIT | PureWellness LLC | 25db8c55-0fa9-4795-8e05-4d3a7aaf0148 | 2026-07-06 | Warnings | 87817-101-01 87817010101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.