FDA.reportPublic FDA data

NDC11 43742218401

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 NDCProduct root
43742-2184-0143742-2184
43742-2184-143742-2184

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 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Menopause ReliefADENOSINUM TRIPHOSPHORICUM DINATRUM, BRYONIA (ALBA), CEDRON, DIM (3, 3-DIINDOLYMETHANE), EQUOL, FAECALIS (ALKALIGENES), IGNATIA AMARA, LACHESIS MUTUS, PETROSELINUM SATIVUM, SANGUINARIA CANADENSIS, SEPIA, STANNUM METALLICUM, SULPHURDeseret Biologicals, Inc.649d19e2-3bed-4d2e-834d-4354a90d87e62024-08-14WarningsExact identifier
ndc (package): 43742-2184-1
ndc (product): 43742-2184
ndc11 (package): 43742218401

Reported adverse events (FAERS/openFDA)#

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