FDA.reportPublic FDA data

NDC11 10596033735

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
10596-0337-3510596-0337
10596-337-3510596-337

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
Ban Roll-On Antiperspirant Deodorant Powder FreshALUMINUM CHLOROHYDRATEKao USA Inc.b99e8972-24e6-4f01-80f5-d071bbab8d302024-10-08WarningsExact identifier
ndc (package): 10596-337-35
ndc (product): 10596-337
ndc11 (package): 10596033735