NDC11 43742211901

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
43742-2119-01	43742-2119
43742-2119-1	43742-2119

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
Skin Infections	AILANTHUS GLANDULOSUS, ARSENICUM ALBUM, HERPES SIMPLEX VIRUS 1 AND 2 DNA, ECHINACEA (ANGUSTIFOLIA), HEPAR SULPHURIS CALCAREUM, HERPES SIMPLEX I AND II NOSODE, HERPES ZOSTER NOSODE, LACHESIS MUTUS, MERCURIUS SOLUBILIS, MEZEREUM, PHYTOLACCA DECANDRA	Deseret Biologials, Inc.	0f19e615-81a2-49d7-a2fa-a9b18b2edb79	2024-08-30	Warnings	Exact identifier ndc (package): 43742-2119-1 ndc (product): 43742-2119 ndc11 (package): 43742211901

Reported adverse events (FAERS/openFDA)#

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