FDA.reportPublic FDA data

FDA label 18a4c3f0-c2d2-4cae-9389-444ad9c83393

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
80f442ba-e968-4fad-ae41-fa1992008ca4
SPL ID
18a4c3f0-c2d2-4cae-9389-444ad9c83393
Version
3
Effective date
2011-07-20
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:49:57

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: If side-effects, such as redness, itching or swelling occur, discontinue use. If a irritation continues after discontinuing use, consult a dermatologist. If a red area develops using this product or there is swelling or itchiness, consult a dermatologist. Exposure to direct sunlight may cause side-effects as above. Do not apply product to an area of skin that is affected by eczema or dermatitis. Wash eyes immediately and thoroughly if product enters eyes.

Reported adverse events (FAERS/openFDA)#

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