NDC11 43742220201

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
43742-2202-01	43742-2202
43742-2202-1	43742-2202

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
Bio Galium Phase	APIS MELLIFICA, ARGENTUM METALLICUM, AURUM METALLICUM, CALCAREA FLUORICA, CALTHA PALUSTRIS, CLEMATIS ERECTA, CORTISONE ACETICUM, ECHINACEA (ANGUSTIFOLIA), GAERTNER BACILLUS (BACH), GALIUM APARINE, HEDERA HELIX, JUNIPERUS COMMUNIS, NITRICUM ACIDUM, ONONIS SPINOSA, PHOSPHORUS, SEDUM ACRE, SEMPERVIVUM TECTORUM, THUJA OCCIDENTALIS, URTICA URENS	Deseret Biologicals, Inc.	902f38c5-b870-4313-9b0b-e69ca357d844	2026-01-09	Warnings	Exact identifier ndc (package): 43742-2202-1 ndc (product): 43742-2202 ndc11 (package): 43742220201

Reported adverse events (FAERS/openFDA)#

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