FDA label 075705f5-2407-5db4-e063-6294a90a3916

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
53e2811c-e17a-4474-b9ef-4a76e6e24b63
SPL ID
075705f5-2407-5db4-e063-6294a90a3916
Version
4
Effective date
2023-10-10
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:23:29

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.