FDA label 07574155-0fb3-d615-e063-6394a90acaaf

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
36328985-ba41-4c8a-8a73-2bb813a830d7
SPL ID
07574155-0fb3-d615-e063-6394a90acaaf
Version
4
Effective date
2023-10-10
Source export date
2026-09-28
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/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:17:36

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 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 •redness is present •side effects occur. If pregnant, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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