FDA label 3dcac1b9-0103-4c58-b3d0-df808a739262

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
905152c2-aa08-4187-87f4-f47f5468041f
SPL ID
3dcac1b9-0103-4c58-b3d0-df808a739262
Version
8
Effective date
2010-08-23
Source export date
2026-10-12
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:29:18

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 WITH A HEATING PAD KEEP AWAY FROM CHILDREN TO AVOID ACCIDENTAL POISONING DO NOT BANDAGE TIGHTLY DO NOT SWALLOW If swallowed, induce vomiting and call a physician. Keep away from eyes and mucous membranes Do not apply to wounds or broken, damaged or irritated skin. If condition worsens, skin redness or irritation develops, or pain lasts more than 7 days, discontinue use and call a physician For arthritis-like conditions in children under 12, do not use and call a physician.

Reported adverse events (FAERS/openFDA)#

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