Menthozen Hydrogel

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 Hydrogel
Generic name
MENTHOL, CAPSAICIN
Manufacturer
Village Pharma LLC
Product type
HUMAN OTC DRUG
SPL set ID
4c979a71-7c8f-4dff-abae-bf4cdf8f67b4
SPL ID
0b180d0a-7ca6-49f9-801f-ca011791a565
Version
3
Effective date
2026-01-01
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:28:58
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. Use only as directed. • Avoid contact with eyes and mucous membranes. • Do not apply to open wounds or damaged skin. Do not use • in combination with any external heat source. • Do not use on irritated or broken skin, or use in combination with any bandage, wrap, stocking or similar device or garment. Keep out of reach of children. • Do not use if allergic to Menthol. Stop use and consult physician • if symptoms worsen or persist for more than 7 days. • Stop use if itching or excessive skin irritation occurs. If pregnant or breast feeding, • contact physician prior to use

Reported adverse events (FAERS/openFDA)#

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