Menthozen

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
Menthozen
Generic name
METHYL SALICYLATE, MENTHOL, CAPSAICIN
Manufacturer
Village Pharma LLC
Product type
HUMAN OTC DRUG
SPL set ID
48b1b99e-d0ec-4e5c-b80c-c0d2d87ecb13
SPL ID
49124ae3-42ed-4a76-a091-ac46529ed235
Version
4
Effective date
2026-01-01
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:14:34
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. • Avoid contact with the eyes. • If condition worsens, or if symptoms persist for more than seven days or clear up and occur again with a few days, discontinue use of this product and consult a physician. Keep out of reach of children. If swallowed, consult physician. Do not apply • to wounds or damaged skin. • Do not bandage tightly. If pregnant or breast feeding, contact a physician prior to use.

Reported adverse events (FAERS/openFDA)#

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