NDC11 83570000302

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
83570-0003-02	83570-0003
83570-0003-2	83570-0003
83570-003-02	83570-003

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
Pain Relief	MENTHOL SPRAY	Owell Naturals Brand, LLC	534c871c-da35-6135-e063-6294a90aa9f6	2026-06-02	Warnings	Exact identifier ndc (package): 83570-003-02 ndc (product): 83570-003 ndc11 (package): 83570000302

Reported adverse events (FAERS/openFDA)#

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