NDC11 84253000101

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
84253-0001-01	84253-0001
84253-0001-1	84253-0001
84253-001-01	84253-001

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
FEMININE PAIN RELIEF	MENTHOL, UNSPECIFIED FORM	BeYou Together Ltd	9636b973-fe7e-481e-a6e9-8070347c0883	2025-12-31	Warnings	Exact identifier ndc (package): 84253-001-01 ndc (product): 84253-001 ndc11 (package): 84253000101

Reported adverse events (FAERS/openFDA)#

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