NDC11 59469020310

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
59469-0203-1059469-0203
59469-203-1059469-203

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
VULPURSILVER NITRATE, ARMORACIA RUSTICANA WHOLE, CINNAMOMUM VERUM WHOLE, WOOD CREOSOTE, CAPSELLA BURSA-PASTORIS, CALENDULA OFFICINALIS FLOWERING TOP, ACHILLEA MILLEFOLIUM, AND SALVIA OFFICINALIS FLOWERING TOPPEKANA Naturheilmittel GmbH19425603-1b4c-4e2c-8980-032b2de98fe82022-12-20WarningsExact identifier
ndc (package): 59469-203-10
ndc (product): 59469-203
ndc11 (package): 59469020310

Reported adverse events (FAERS/openFDA)#

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