NDC11 71753125801
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 |
|---|---|
| 71753-1258-01 | 71753-1258 |
| 71753-1258-1 | 71753-1258 |
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 |
|---|---|---|---|---|---|---|
| Virus Defense ANNAKARE | ACONITUM NAPELLUS ROOT, ARSENIC TRIOXIDE, BAPTISIA TINCTORIA WHOLE, BRYONIA ALBA ROOT, ECHINACEA ANGUSTIFOLIA WHOLE, EUPATORIUM PERFOLIATUM WHOLE, GELSEMIUM SEMPERVIRENS WHOLE, GLYCYRRHIZA GLABRA, HYDRASTIS CANADENSIS WHOLE, TOXICODENDRON PUBESCENS LEAF | Ratis, LLC | 147f3bee-0fbc-472d-aade-90897550b836 | 2025-10-03 | Warnings | 71753-1258-1 71753-1258 71753125801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.