FDA.reportPublic FDA data

FDA label e77e9f10-33f3-49c0-804f-c026653b1826

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
e495f18f-4c42-4126-a4c2-f5641aa163a7
SPL ID
e77e9f10-33f3-49c0-804f-c026653b1826
Version
2
Effective date
2016-07-18
Source export date
2026-10-12
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:26:09

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 eyes and mucous membranes. Do not apply to open wounds or damaged skin or use with a heating pad. Does not require additional cover bandage. Do not use if allergic or sensitive to Menthol or Lidocaine. Stop use and ask a doctor if condition worsen, symptoms persist for more than 7 days. Stop use and ask a doctor if condition worsen, symptoms persist for more than 7 days or clear up and occur again within a few days. Contact physician if rash, blistering, itching or excessive skin irritation occurs. If swallowed, consult physician. If pregnant or breast feeding, contact a physician prior to use. KEEP OUT OF REACH OF CHILDREN.

Reported adverse events (FAERS/openFDA)#

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