FDA label 36efd53e-5462-4c5b-8c81-1ceefdd66b4a

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)

SPL set ID
bc04d761-56b8-43fc-926b-fb8e3c3da48b
SPL ID
36efd53e-5462-4c5b-8c81-1ceefdd66b4a
Version
4
Effective date
2021-07-01
Source export date
2026-11-06
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/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:48:56

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 withy 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 irrigation 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.