NDC11 43742206101

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
43742-2061-01	43742-2061
43742-2061-1	43742-2061

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
ENT Support	PULSATILLA (PRATENSIS), EUPHORBIUM OFFICINARUM, LUFFA OPERCULATA, MERCURIUS IODATUS RUBER, ARGENTUM NITRICUM, HEPAR SULPHURIS CALCAREUM, INFLUENZINUM (2022-2023), SINUSITISINUM, ASPERGILLUS NIGER, CANDIDA ALBICANS, GALLICUM ACIDUM, MUCOR RACEMOSUS, MUTABILE BACILLUS (BACH)	Deseret Biologicals, Inc.	be9efe32-f461-4d33-92ee-852069533176	2024-01-15	Warnings	Exact identifier ndc (package): 43742-2061-1 ndc (product): 43742-2061 ndc11 (package): 43742206101

Reported adverse events (FAERS/openFDA)#

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