FDA label 23b6f61e-b524-43fc-9b0a-b4c34d810f92

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
a99336b9-05fa-467b-80d2-64de8a841cf6
SPL ID
23b6f61e-b524-43fc-9b0a-b4c34d810f92
Version
2
Effective date
2017-09-07
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:07:25

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 Warnings 1. If you experience any of the following symptoms after using this product, you are advised to stop using it immediately. If symptoms persist, consult a dermatologist. 1) red rash, swollenness, itching tingling during use. 2) any of the above symptoms when area of application is exposed to direct sunlight. 2. Do not use on areas of the skin with scarring, eczema or dermatitis. 3. Avoid contact with eyes. In case of contact with eyes, rinse eyes immediately with water.

Reported adverse events (FAERS/openFDA)#

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