CVS 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
CVS Pain Relief
Generic name
MENTHOL 4%
Manufacturer
CVS
Product type
HUMAN OTC DRUG
SPL set ID
d1660d55-1ee0-7aa2-e053-2995a90a6579
SPL ID
28f15d7e-f9cc-4807-e063-6294a90ab6f7
Version
3
Effective date
2024-12-11
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:31:16
Harmonized routes table
Harmonized routes
TOPICAL

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

For external use only Flammable: Keep away from excessive heat or open flame Ask a doctor before use if you have : sensitive skin Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days. When using this product Use only as directed Avoid contact with eyes or mucous membranes Do not apply to wounds or damaged skin Do not use with other ointments, creams, sprays or liniments Do not apply to irritated skin or if excessive irritation develops Do not bandage or use with heating pad or device Store in a cool dry place away from direct sunlight Wash hands after use with cool water If pregnant or breastfeeding , ask a health professional before use Keep out of reach of children: If accidentally ingested, get medical help or contact a poison Control immediately (1800-222-1222)

Reported adverse events (FAERS/openFDA)#

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