FDA label 4c2de5b4-bcf0-4e79-b65e-64e87b28f331

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
30d6241f-9fca-4a1a-a509-1274007debb3
SPL ID
4c2de5b4-bcf0-4e79-b65e-64e87b28f331
Version
4
Effective date
2026-07-24
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:56:40

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.