FDA.reportPublic FDA data

FDA label 995e72be-ae27-4098-9169-bda522798cf3

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
994b5ded-0098-4887-829c-cc64481b7f8e
SPL ID
995e72be-ae27-4098-9169-bda522798cf3
Version
1
Effective date
2015-11-16
Source export date
2026-09-28
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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:41:34

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. Please stop using the product while you find the following symptoms, otherwise it will worsen and get needed to consult dermatological specialist. a) Red dots, Swelling, Irritation and pains while you are using the product. b) Above symptoms happen at direct sunlight. 2. Please do not use on wound, eczema or inflammation area. 3. Keeping caution a) Please close the cap after use. b) Please keep away from babies and children. c) Please do not keep on high or low temperature or under direct sunlight 4. Please do not apply on the area the eyes.

Reported adverse events (FAERS/openFDA)#

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