NDC11 43742153801

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
43742-1538-0143742-1538
43742-1538-143742-1538

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
Skin InfectionsECHINACEA (ANGUSTIFOLIA), PHYTOLACCA DECANDRA, HEPAR SULPHURIS CALCAREUM, MERCURIUS SOLUBILIS, MEZEREUM, AILANTHUS GLANDULOSUS, ARSENICUM ALBUM, LACHESIS MUTUS, HERPES SIMPLEX I AND II NOSODE, HERPES ZOSTER NOSODEDeseret Biologials, Inc.43eb02e6-723c-4ab5-81cf-4ab18da8d3ea2024-02-02WarningsExact identifier
ndc (package): 43742-1538-1
ndc (product): 43742-1538
ndc11 (package): 43742153801

Reported adverse events (FAERS/openFDA)#

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