FDA label 8c11b9d5-2ef4-411c-84c3-7c9ccf06ae11

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
bdbd4106-e4fe-4daf-a757-3aee3a87bb09
SPL ID
8c11b9d5-2ef4-411c-84c3-7c9ccf06ae11
Version
2
Effective date
2017-09-08
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:33:32

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 •more than one patch on your body at a time or on cut •on wounds or damaged skin •with a heating pad When using this product •avoid contact with eyes, mucous membranes or rashes •use only as directed •do not bandage tightly •do not use at the same time as other topical analgesics •dispose of used patch in a manner that always keeps products away from children and pets Stop use and ask a doctor if •you experience signs of skin injury, such as pain, swelling or blistering where product was applied •symptoms persist for more than 7 days or clear up and occur again within a few days •condition worsens •redness is present •irritation develops

Reported adverse events (FAERS/openFDA)#

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