NDC11 57955998202
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 |
|---|---|
| 57955-9982-02 | 57955-9982 |
| 57955-9982-2 | 57955-9982 |
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 |
|---|---|---|---|---|---|---|
| Arthritis Pain and Joint Relief | ACTAEA SPICATA, AESCULUS HIPPOCASTANUM, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA, CALCAREA CARBONICA, CALCAREA FLUORICA, CAUSTICUM, CIMICIFUGA RACEMOSA, FORMICUM ACIDUM, HYPERICUM PERFORATUM, LEDUM PALUSTRE, LITHIUM CARBONICUM, MAGNESIA PHOSPHORICA, PHOSPHORUS, PHYTOLACCA DECANDRA, PULSATILLA, RHODODENDRON CHRYSANTHUM, RHUS TOX, RUTA GRAVEOLENS, SALICYLICUM ACIDUM, SEPIA AND ZINCUM METALLICUM. | King Bio Inc. | 8ecb7378-ea84-483c-ba1c-852d1ae7b90d | 2026-03-02 | Warnings | 57955-9982-2 57955-9982 57955998202 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.