NDC11 43857060201

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
43857-0602-01	43857-0602
43857-0602-1	43857-0602
43857-602-01	43857-602

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
Jointforce R	CHONDRUS CRISPUS, CIMICIFUGA RACEMOSA, SPIRAEA ULMARIA, TRIFOLIUM PRATENSE, URTICA URENS, XANTHOXYLUM FRAXINEUM, SYMPHYTUM OFFICINALE, COLCHICUM AUTUMNALE, FERRUM PHOSPHORICUM, FORMICA RUFA, LITHIUM CARBONICUM, NATRUM SULPHURICUM, RHODODENDRON CHRYSANTHEMUM, RHUS TOX	BioActive Nutritional, Inc.	26a45f44-4c9e-420d-aa76-9d3a67326d12	2026-03-05	Warnings	Exact identifier ndc (package): 43857-0602-1 ndc (product): 43857-0602 ndc11 (package): 43857060201

Reported adverse events (FAERS/openFDA)#

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