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
20234356-5e80-b79e-e063-6294a90a2ee3
SPL ID
23aaba32-8d1b-6a5b-e063-6394a90a3adc
Version
2
Effective date
2024-10-04
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:32:56
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. When using this product use only as directed. Avoid contact with eyes and mucous membranes, do not apply to wounds or damaged skin, do no apply to irritated skin or if excessive irritation develops, do not bandage tightly or use with heating pad or device. Children 12 years of age and older: use only under adult supervision. Stop use and ask a doctor if you experience pain, swelling, or blistering of the skin, condition worsens, symptoms last 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.