FDA label d1d56938-35ce-4d01-a276-12fc3d846772

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
d0095fc8-c7d4-4a16-96e7-d46687c31568
SPL ID
d1d56938-35ce-4d01-a276-12fc3d846772
Version
2
Effective date
2023-03-15
Source export date
2026-10-12
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/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:47:59

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 with a heating pad on a child under 12 years of age with arthritis – like conditions Ask a doctor before use if you have redness over affected area When using this product • Avoid contact with eyes or mucous membranes. Do not bandage tightly. • Stop use and ask a doctor if condition worsens or symptoms persists for more than 7 days. • Symptoms clear up and occur again within a few days. • Excessive skin irritation occurs. 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.