NDC11 57955998402

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 table
Package NDC	Product root
57955-9984-02	57955-9984
57955-9984-2	57955-9984

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Back, Muscle and Joint Relief	AESCULUS HIPPOCASTANUM, ARNICA MONTANA, BELLIS PERENNIS, BRYONIA, CALCAREA CARBONICA, CALCAREA FLUORICA, CIMICIFUGA RACEMOSA, COBALTUM METALLICUM, GNAPHALIUM POLYCEPHALUM, HYPERICUM PERFORATUM, KALI CARBONICUM, KALI PHOSPHORICUM, MAGNESIA PHOSPHORICA, OXALICUM ACIDUM, PHOSPHORUS, RHUS TOX, RUTA GRAVEOLENS, AND ZINCUM METALLICUM.	King Bio Inc.	c6e50f93-bc45-4755-8ab0-dbe0d9987fca	2026-03-02	Warnings	Exact identifier ndc (package): 57955-9984-2 ndc (product): 57955-9984 ndc11 (package): 57955998402

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.