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
Manufacturer: Pain Relieving Spray Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 1f44466f-044f-70fe-e063-6294a90ad575
SPL ID: 1f44466f-0450-70fe-e063-6294a90ad575
Version: 1
Effective date: 2024-08-09
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:18:45

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	openfda.generic_name
manufacturer name		Pain Relieving Spray Inc.	openfda.manufacturer_name
ndc	package	84638-8201-1	openfda.package_ndc
ndc	product	84638-8201	openfda.product_ndc
ndc11	package	84638820101	derived:openfda.package_ndc
rxcui		1086713	openfda.rxcui
spl id		1f44466f-0450-70fe-e063-6294a90ad575	id
spl set id		1f44466f-044f-70fe-e063-6294a90ad575	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

Warning For external use only. Flammable Keep away from flame. Keep out of reach of children. If swallowed get medical help or contact a poison control center right away. Avoid contact with eyes. Do not apply to open wounds or damaged skin. Do not bandage tightly. Consult a doctor if excessive skin irritation occurs, or if you are prone to allergic reactions to salicylates,including aspirin. If condition worsens, if symptoms persist for more than 7 days or clear up and recur again within a few days, discontinue use of this product and consult a doctor.

Reported adverse events (FAERS/openFDA)#

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