FDA.reportPublic FDA data

FDA label 3960065b-cbaa-79b9-e063-6294a90afbbb

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
3dfeb1d0-f813-2eaa-e054-00144ff88e88
SPL ID
3960065b-cbaa-79b9-e063-6294a90afbbb
Version
4
Effective date
2025-07-07
Source export date
2026-09-28
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:12:39

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

Warning For external use only When using this product Use only as directed Read and follow all directions and warnings on this label Rare cases of serious burns have been reported with products of this type Do not bandage tightly or apply local heat (such as heating pads)or medicated patches to the area of use Avoid contact with eyes and mucous membranes Do not apply to wounds or damages, broken or irritated skin A trasient burning sensation may occur upon application but generally dissapears in several days

Reported adverse events (FAERS/openFDA)#

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