FDA.reportPublic FDA data

FDA label 6613842a-e72d-4cd3-bc77-116df9161a99

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
ed7ee9b0-c64f-4c46-a08f-dc47fe73c381
SPL ID
6613842a-e72d-4cd3-bc77-116df9161a99
Version
1
Effective date
2014-01-07
Source export date
2026-11-06
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/245ea1c0d730b312e4410f082201cbe2cb4d1936fa2918316b6ea631293cbeba/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 08:05:32

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, damaged, broken or irritated skin with a heating pad When using this product use only as directed avoid contact with eyes or mucous membranes Do not apply bandage tightly Stop use and ask doctor if Condition worsens, or symtoms persist for more than 7 days symptoms clear up and occur again within a few days excessive skin irritation occurs If pregnant or breast feeding , ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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