Medline

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
Medline
Generic name
MENTHOL
Manufacturer
Medline Industries, LP
Product type
HUMAN OTC DRUG
SPL set ID
0d947aa6-045e-d001-e063-6294a90a3657
SPL ID
387c2d55-f00b-422f-e063-6294a90a898e
Version
2
Effective date
2025-06-26
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 03:10:08
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

Warnings For external use only Ask doctor before use if you have: sensitive skin When using this product use only as directed do not bandage tightly or use with heating pad or device do not apply to wounds or damaged skin do not use with other ointments, creams, sprays, or liniments do not apply to irritated skin avoid contact with eyes, mucous membranes or rashes Stop use and ask a doctor if burning discomfort or excessive skin irritation develops condition worsens symptoms persist for more than 7 days symptoms clear up and occur again within a few days If pregnant or breast-feeding, ask a health professional before use 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.