FDA label 4adb8ea5-da26-45b5-bffb-6d1536090786

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
2dccf5b6-98e1-4bf0-9c70-e3b37c468446
SPL ID
4adb8ea5-da26-45b5-bffb-6d1536090786
Version
2
Effective date
2026-07-27
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:47:09

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. Do not use otherwise than as directed. Do Not Use On open wounds, cuts, eyes and face With a heating pad When using this product Avoid contact with eyes and mucous membranes Do not bandage tightly Ask Your Doctor Before Use if you have redness over the affected area have sensitive skin are pregnant or breast-feeding Stop Use and Ask Your Doctor If condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days If abnormal skin irritation occurs after usage Keep Out of Reach of Children. If swallowed, seek medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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