FDA.reportPublic FDA data

FDA label 3d92574b-3274-49d2-e054-00144ff8d46c

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
c15809b0-5d14-45c4-8c2d-9856ef0e8416
SPL ID
3d92574b-3274-49d2-e054-00144ff8d46c
Version
3
Effective date
2016-09-28
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:30:16

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. • Consult physician for children under 12. • 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 to 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.