NDC11 71753115601
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 |
|---|---|
| 71753-1156-01 | 71753-1156 |
| 71753-1156-1 | 71753-1156 |
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 |
|---|---|---|---|---|---|---|
| Cold Armor | ALLIUM CEPA, HYDRASTIS CANADENSIS, PULSATILLA (PRATENSIS), DULCAMARA, NUX VOMICA, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, KALI BICHROMICUM | Ratis, LLC | 46af3f19-055e-4025-a14e-1d6c25880f4d | 2023-05-26 | Warnings | 71753-1156-1 71753-1156 71753115601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.