NDC11 71726000501

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
71726-0005-01	71726-0005
71726-0005-1	71726-0005
71726-005-01	71726-005

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
FREEZE IT Menthol Roll On	MENTHOL	LiquidCapsule Manufacturing LLC	33094afe-db9d-4b92-8047-6dd611484fc9	2025-06-05	Warnings	Exact identifier ndc (package): 71726-005-01 ndc (product): 71726-005 ndc11 (package): 71726000501

Reported adverse events (FAERS/openFDA)#

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