NDC11 10565006602

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
10565-0066-02	10565-0066
10565-0066-2	10565-0066
10565-066-02	10565-066

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
Roll On Anti Perspirant Alcohol Free	ALUMINUM CHLOROHYDRATE	Hydrox Laboratories	c5fb6769-23a3-4738-afe7-5ebbca4d9e69	2026-01-12	Warnings	Exact identifier ndc (package): 10565-066-02 ndc (product): 10565-066 ndc11 (package): 10565006602

Reported adverse events (FAERS/openFDA)#

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