Equate Menthol Pain Relieving

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
Equate Menthol Pain Relieving
Generic name
MENTHOL
Manufacturer
Wal-Mart Stores Inc
Product type
HUMAN OTC DRUG
SPL set ID
d5b0a7f1-4e23-426b-bb7e-aaa251ad4ffc
SPL ID
5a98d4a1-d1fa-355a-e063-6294a90a2f5b
Version
6
Effective date
2026-09-03
Source export date
2026-09-28
Source partition
14
Source file
https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:41:43
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only When using this product use only as directed avoid contact with eyes and mucous membranes do not apply to wounds or to damaged or very sensitive skin do not bandage tightly or use with a heating pad Stop use and ask a doctor if condition worsens excessive redness, irritation, burning, or discomfort of the skin develops symptoms persist for more than 7 days or clear up and occur again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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