NDC11 84878019901

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
84878-0199-0184878-0199
84878-0199-184878-0199
84878-199-0184878-199

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
Sunsolve MD Firm and ReplenishZINC OXIDESunsolve MD Inc26f3417b-9ea4-e577-e063-6294a90ae53c2025-11-14WarningsExact identifier
ndc (package): 84878-199-01
ndc (product): 84878-199
ndc11 (package): 84878019901

Reported adverse events (FAERS/openFDA)#

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