NDC11 10596033914

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 NDC	Product root
10596-0339-14	10596-0339
10596-339-14	10596-339

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ban Roll-On Antiperspirant Deodorant Satin Breeze	ALUMINUM CHLOROHYDRATE	Kao USA Inc.	d6d6368f-489f-4d6b-bbc0-e2dfb7ec3f90	2024-09-06	Warnings	Exact identifier ndc (package): 10596-339-14 ndc (product): 10596-339 ndc11 (package): 10596033914

Reported adverse events (FAERS/openFDA)#

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