FDA.reportPublic FDA data

FDA label 1a4c0e56-b4cb-682b-e054-00144ff88e88

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
1a4cf25c-8e83-68c8-e054-00144ff8d46c
SPL ID
1a4c0e56-b4cb-682b-e054-00144ff88e88
Version
4
Effective date
2015-07-07
Source export date
2026-11-06
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:57:03

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 . Use only as directed Do not bandage tightly Do not use with a heating pad Avoid contact with the eyes or mucous membranes Do not apply to wounds, damaged, broken or irritated skin A transient burning sensation may occur upon application but generally disappears in several days If severe burning sensation occurs, discontinue use immediately and call a doctor Do not expose the area treated with product to heat or direct sunlight

Reported adverse events (FAERS/openFDA)#

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