FDA label 710fa724-ab4e-4f39-b827-a533213c1773

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
0f9d82be-de77-42a9-a6ee-1778846bdf81
SPL ID
710fa724-ab4e-4f39-b827-a533213c1773
Version
2
Effective date
2015-05-08
Source export date
2026-10-12
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:23:27

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 or damaged skin. if you are allergic to aspirin or salicylates. with a heating pad. with, or at the same times as, other external analgesic products. Ask a doctor before use, if you are allergic to any ingredients of this product. When using this product do not use otherwise than as directed. avoid contact with the eyes, mucous membranes or rashes. do not bandage tightly. Stop use and ask a doctor if rash, itching or excessive skin irritation develops. conditions worsen. symptoms persist for more than 7 days. symptoms clear up and occur again within a few days. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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