FDA.reportPublic FDA data

NDC11 00316026401

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
00316-0264-0100316-0264
00316-0264-100316-0264
00316-264-0100316-264
0316-0264-010316-0264

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
PanOxylBENZOYL PEROXIDECrown Laboratoriesff09cbab-304b-4da9-e053-6394a90ae6002026-01-12WarningsExact identifier
ndc (package): 0316-0264-01
ndc (product): 0316-0264
ndc11 (package): 00316026401

Reported adverse events (FAERS/openFDA)#

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