FDA.reportPublic FDA data

NDC11 59088043510

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
59088-0435-1059088-0435
59088-435-1059088-435

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage59088-43559088-435-10IInactivated by FDA2026-07-31

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LextolDICLOFENAC SODIUM, CAPSAICINPureTek Corporation042765e5-bd75-8224-e063-6394a90a141b2025-12-19Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 59088-435-10
ndc11 (package): 59088043510
DiclogenDICLOFENAC SODIUM, CAMPHOR AND MENTHOLPureTek Corporation1e2bb4e5-bb65-48a0-e063-6294a90a54d12025-12-18Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 59088-435-10
ndc11 (package): 59088043510
LixofenDICLOFENAC SODIUM, KINESIOLOGY TAPEPureTek Corporation1e2a687b-a838-9b16-e063-6394a90a69f32025-12-18Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 59088-435-10
ndc11 (package): 59088043510