FDA label 8e7480a9-2466-4a03-9bba-bdc56a8535f9

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
cdb215cc-71e5-43e7-a044-d264a9321257
SPL ID
8e7480a9-2466-4a03-9bba-bdc56a8535f9
Version
3
Effective date
2013-11-19
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:30:16

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 When using this product use only as directed do not bandage tightly or use with a heating pad do not use on irritated, wounded or damaged skin avoid contact with eye or mucous membranes Do not use if you are allergic to fragrance you have asthma you are pregnant or breast-feeding Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days redness is present irritation develops Keep out of reach of children If patch is swallowed, get medical help or contact poison control center immediately.

Reported adverse events (FAERS/openFDA)#

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