NDC11 55714259201
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 |
|---|---|
| 55714-2592-01 | 55714-2592 |
| 55714-2592-1 | 55714-2592 |
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 |
|---|---|---|---|---|---|---|
| Vitiligo | ECHINACEA, IRIS VERSICOLOR, RUMEX CRISPUS, BERBERIS VULGARIS, BOVISTA, DOLICHOS PRURIENS, HURA BRASILIENSIS, HYDROCOTYLE ASIATICA, LYCOPODIUM CLAVATUM, MEZEREUM, RHUS TOXICODENDRON, SEPIA, TARAXACUM OFFICINALE, THUJA OCCIDENTALIS, URTICA URENS, ARSENICUM ALBUM | Newton Laboratories, Inc. | 136945e2-6f2a-a0df-e063-6294a90a994b | 2024-03-11 | Warnings | 55714-2592-1 55714-2592 55714259201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.