NDC11 70163000801

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
70163-0008-0170163-0008
70163-0008-170163-0008
70163-008-0170163-008

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
VertiFixARGENTUM NITRICUM, BRYONIA (ALBA), CAUSTICUM, COCCULUS INDICUS, GELSEMIUM SEMPERVIRENS, IPECACUANHA, NUX VOMICA, PETROLEUM, SULPHUR, TABACUMNaturalCare33b00f06-3202-4904-855c-cdfaa93677a42026-08-27WarningsExact identifier
ndc (package): 70163-0008-1
ndc (product): 70163-0008
ndc11 (package): 70163000801

Reported adverse events (FAERS/openFDA)#

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