FDA.reportPublic FDA data

FDA label 1a4afc2e-1d78-2243-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
1a4afc2e-1d77-2243-e054-00144ff88e88
SPL ID
1a4afc2e-1d78-2243-e054-00144ff88e88
Version
1
Effective date
2015-07-07
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:35:14

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 2 matching rows.

warnings and cautions

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

warnings and cautions

STOP USE AND ASK A DOCTOR IF: Condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days Redness is present or irritation develops

Reported adverse events (FAERS/openFDA)#

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