FDA.reportPublic FDA data

NDC11 43742208301

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
43742-2083-0143742-2083
43742-2083-143742-2083

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
Eye SupportALLIUM CEPA, SYMPHYTUM OFFICINALE, ARGENTUM NITRICUM, EYE (SUIS), VACCINIUM MYRTILLUS, APIS MELLIFICA, CALCAREA FLUORICA, CARBONEUM SULPHURATUM, CEDRON, GELSEMIUM SEMPERVIRENS, KALI IODATUM, NUX MOSCHATA, PHOSPHORUS, PHYSOSTIGMA VENENOSUM, STAPHYSAGRIADeseret Biologicals, Inc.dd8484aa-5bb7-490c-8586-c2bf6a5d02bb2024-10-23WarningsExact identifier
ndc (package): 43742-2083-1
ndc (product): 43742-2083
ndc11 (package): 43742208301

Reported adverse events (FAERS/openFDA)#

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