FDA label 075774dc-d6de-0ff1-e063-6294a90a0b0b

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
7e8c918a-e3b7-4b0f-89ce-def8bc8d7406
SPL ID
075774dc-d6de-0ff1-e063-6294a90a0b0b
Version
4
Effective date
2023-10-10
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 05:23:42

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 •on wounds •irritated or damaged skin •sensitive skin •with a heating pad •if pregnant •with, or as the same time as, other external analgesic products •if allergic to aspirin or salicylates •if allergic to any ingredients of this product When using this product •avoid contact with the eyes •do not bandage tightly •do not apply to wounds or damaged skin •do not use more than 3 plasters a day •do not use 1 hour before or after bathing 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 •rashes, itching or redness are present •side effects occur. You may call: 1-800-617-2021 If pregnant, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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