NDC11 55714483001
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 |
|---|---|
| 55714-4830-01 | 55714-4830 |
| 55714-4830-1 | 55714-4830 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 55714-4830 | 55714-4830-1 | U | Excluded because listing certification expired | excluded / ndc_excluded.zip | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 55714-4830 | 55714-4830-1 | U | Excluded because listing certification expired | excluded / ndc_excluded.zip | 0efc9e666f02… | f202fb6c5f17… |
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 |
|---|---|---|---|---|---|---|
| Viral | ECHINACEA, HYDRASTIS CANADENSIS, ACONITUM NAPELLUS, ANTIMONIUM TARTARICUM, ARNICA MONTANA, ARSENICUM ALBUM, BAPTISIA TINCTORIA, BELLADONNA, BRYONIA, CANTHARIS, CHAMOMILLA, GAULTHERIA PROCUMBENS, HEPAR SULPHURIS CALCAREUM, IODIUM, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, MERCURIUS VIVUS, PHOSPHORUS, PULSATILLA, RHUS TOXICODENDRON, TRIFOLIUM PRATENSE, INFLUENZINUM, MORBILLINUM. | Newton Laboratories, Inc. | 9a673e6b-e0d7-77c2-e053-2995a90ac766 | 2020-12-07 | Warnings | 55714-4830-1 55714-4830 55714483001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.