Pain Relief

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Pain Relief
Generic name: MENTHOL SPRAY
Manufacturer: Owell Naturals Brand, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 534c871c-da35-6135-e063-6294a90aa9f6
SPL ID: 534c871c-da36-6135-e063-6294a90aa9f6
Version: 1
Effective date: 2026-06-02
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:17:50

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Pain Relief	openfda.brand_name
generic name		MENTHOL SPRAY	openfda.generic_name
manufacturer name		Owell Naturals Brand, LLC	openfda.manufacturer_name
ndc	package	83570-003-02	openfda.package_ndc
ndc	product	83570-003	openfda.product_ndc
ndc11	package	83570000302	derived:openfda.package_ndc
rxcui		2744629	openfda.rxcui
spl id		534c871c-da36-6135-e063-6294a90aa9f6	id
spl set id		534c871c-da35-6135-e063-6294a90aa9f6	set_id
unii		L7T10EIP3A	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS For external use only. Flammable: Keep away from fire or flame. Do not use on wounds or damaged skin. When using this product: Avoid contact with eyes or mucous membranes. Do not bandage tightly. Stop use and ask a doctor if: Condition worsens, symptoms persist for more than 7 days, or clear up and occur again within a few days.

Reported adverse events (FAERS/openFDA)#

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