FDA.reportPublic FDA data

FDA label d6c07729-917f-4a62-8d92-b7c14c745df6

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
4dd046bc-82bf-4790-9d99-01534f391d7f
SPL ID
d6c07729-917f-4a62-8d92-b7c14c745df6
Version
1
Effective date
2015-11-16
Source export date
2026-10-12
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:21:33

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.