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
Proficient Rx LP
Product type
HUMAN OTC DRUG
SPL set ID
85a7809e-c43f-4138-a85b-44e1b586def5
SPL ID
1cdc9d1f-d8eb-40e4-99e6-286c7dbfb986
Version
6
Effective date
2023-12-01
Source export date
2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:08:23
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.