FDA label 2eeaa595-5afb-589f-e054-00144ff8d46c

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
2bbfa904-07a8-0e32-e054-00144ff88e88
SPL ID
2eeaa595-5afb-589f-e054-00144ff8d46c
Version
2
Effective date
2016-03-25
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:23:16

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 • Avoid contact with eyes or mucus membranes • Do not apply to open wounds or damaged skin • If symptoms persist for more than seven days, discontinue use and consult physician • Keep out of reach of children. If swallowed, contact Poison Control Center • Do not bandage tightly • If pregnant or breast feeding, contact physician prior to use • Do not use in large quantities, particularly over raw surfaces or blistered areas • Do not use if excessive irritation of the skin develops • Do not use if condition worsens • Do not use if symptoms clear and occur again within a few days • Do not use if you are allergic to any ingredient in patch.

Reported adverse events (FAERS/openFDA)#

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