NDC11 43742130301

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
43742-1303-01	43742-1303
43742-1303-1	43742-1303

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
Inflammation	ARNICA MONTANA, BENZOICUM ACIDUM, ECHINACEA (ANGUSTIFOLIA), APIS MELLIFICA, BAPTISIA TINCTORIA, DULCAMARA, EUCALYPTUS GLOBULUS, SOLANUM NIGRUM, EUPATORIUM PERFOLIATUM, BRYONIA (ALBA), COLCHICUM AUTUMNALE, MERCURIALIS PERENNIS, RHUS TOX	Deseret Biologicals, Inc.	98578714-8408-4bc0-82ff-faa88cda3757	2024-03-05	Warnings	Exact identifier ndc (package): 43742-1303-1 ndc (product): 43742-1303 ndc11 (package): 43742130301

Reported adverse events (FAERS/openFDA)#

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