Dr PAINES 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: Dr PAINES Pain Relief
Generic name: MENTHOL
Manufacturer: DOCTOR PAINE'S MEDICAL, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 79d2b332-051e-48c1-afe8-6d4468cd1878
SPL ID: 09e235ab-ce28-ad20-e063-6294a90a90a3
Version: 2
Effective date: 2023-11-11
Source export date: 2026-10-30
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/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:26:06

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		Dr PAINES Pain Relief	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		DOCTOR PAINE'S MEDICAL, LLC	openfda.manufacturer_name
ndc	package	78970-161-03	openfda.package_ndc
ndc	product	78970-161	openfda.product_ndc
ndc11	package	78970016103	derived:openfda.package_ndc
rxcui		1039690	openfda.rxcui
spl id		09e235ab-ce28-ad20-e063-6294a90a90a3	id
spl set id		79d2b332-051e-48c1-afe8-6d4468cd1878	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. Avoid contact with eyes. If symptoms persist for more than seven days,discontinue use and consult physician. Keep out of reach of children. If swallowed, consult physician. Do not apply to wounds damaged skin. Do not bandage tightly. If pregnant or breast feeding, contact physician prior to use.

Reported adverse events (FAERS/openFDA)#

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