FDA label b25cbe68-36b1-42b6-a4dd-f18a1149ffab

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
1489dfdd-374e-4b7d-9446-1c5105c7bc5a
SPL ID
b25cbe68-36b1-42b6-a4dd-f18a1149ffab
Version
1
Effective date
2011-03-14
Source export date
2026-10-23
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-23/e2a780351c9d52ec13a8c93757e95e68824c68ebed04761d4eea108c6b76cf54/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
003b0607e7bf4d3ce17ccc0942e221303b4f62b17a6a00c54547eda454293380
Import run
20261026T035824Z
Imported at
2026-10-26 04:31:59

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 the affected area. When using this product - avoid contact with the eyes or mucous membranes - do not bandage tightly Stop use and ask a doctor if - condition worsens or symptoms persist 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.