NDC11 43742197101

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
43742-1971-01	43742-1971
43742-1971-1	43742-1971

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
Immunogesic	ARNICA MONTANA, APIS MELLIFICA, BENZOICUM ACIDUM, CARTILAGO SUIS, LEDUM PALUSTRE, PANTOTHENIC ACID, RUTA GRAVEOLENS, RHODODENDRON CHRYSANTHUM, CAUSTICUM, FORMICA RUFA, SEPIA, ALPHA-LIPOICUM ACIDUM, AURUM METALLICUM, CALCAREA PHOSPHORICA, COLCHICUM AUTUMNALE, PHYTOLACCA DECANDRA, RADIUM BROMATUM, RHUS VENENATA, THUJA OCCIDENTALIS, LAC CANINUM	Deseret Biologicals, Inc.	a7363a92-bcef-450e-9168-39f51a57cf3e	2024-03-07	Warnings	Exact identifier ndc (package): 43742-1971-1 ndc (product): 43742-1971 ndc11 (package): 43742197101

Reported adverse events (FAERS/openFDA)#

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