NDC11 43742214201

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
43742-2142-01	43742-2142
43742-2142-1	43742-2142

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	ARGENTUM NITRICUM, ASPERGILLUS NIGER, CANDIDA ALBICANS, EUPHORBIUM OFFICINARUM, GALLICUM ACIDUM, HEPAR SULPHURIS CALCAREUM, INFLUENZINUM (2023-2024), LUFFA OPERCULATA, MERCURIUS IODATUS RUBER, MUCOR RACEMOSUS, MUTABILE BACILLUS (BACH), PULSATILLA (PRATENSIS), SINUSITISINUM	Deseret Biologicals, Inc.	284327cc-2d06-4f75-a296-52c34f149693	2025-05-27	Warnings	Exact identifier ndc (package): 43742-2142-1 ndc (product): 43742-2142 ndc11 (package): 43742214201

Reported adverse events (FAERS/openFDA)#

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