NDC11 81277000601

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
81277-0006-01	81277-0006
81277-0006-1	81277-0006
81277-006-01	81277-006

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
Sure Regular Antiperspirant and Deodorant	ALUMINUM CHLOROHYDRATE ANHYDROUS	Sodalis USA LLC	46e96649-16c1-4fb9-8ef1-9b9e80fe65c3	2024-11-08	Warnings	Exact identifier ndc (package): 81277-006-01 ndc (product): 81277-006 ndc11 (package): 81277000601

Reported adverse events (FAERS/openFDA)#

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