FDA label 1c5fe04c-b4c4-cbf9-e063-6394a90a37b5

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
1c5fe04c-b4c3-cbf9-e063-6394a90a37b5
SPL ID
1c5fe04c-b4c4-cbf9-e063-6394a90a37b5
Version
1
Effective date
2024-07-03
Source export date
2026-09-28
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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:34:46

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 Allergy aler t: this product contains natural rubber latex which may cause allergic reactions Do not use on wounds on irritated or damaged skin if the appearance of this product has changed if you have known hypersensitivities to this product otherwise than as directed Ask a doctor or pharmacist before use if you are taking other medications pregnant when using this product avoid contact with the eyes or mucous membranes do not bandage tightly do not apply heat to the area in the form of heating pads, hot water bottles, or lamps (the risk of serious burns) avoid placing on extremely hairy areas of skin to avoid irritation upon removing the plaster Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days symptoms clear up and occur again within a few days excessive irritation of the skin develops when using for pain of arthritis: - pain persists for more than 10 days - redness is present - in conditions affecting children under 12 years of age

Reported adverse events (FAERS/openFDA)#

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