FDA label 907474dc-765f-47f5-e053-2a95a90ae0a1

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
90747486-5b0b-69e9-e053-2a95a90ab9ac
SPL ID
907474dc-765f-47f5-e053-2a95a90ae0a1
Version
1
Effective date
2019-08-19
Source export date
2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:51:23

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

Precautions Please stop using this product ifthe following side effects occur.If not, its symptom is worsened. Then please consultdermatologist about it. 1) If it is occurred red spots,itching, stimulation, and others. 2) If it is occurred side effectsas above on the applied partby direct sunlight. Please avoid to be applied it onthe wounded part and the part ofeczema and dermatitis. Warnings in storage andmaintenance. 1) Close a lid after using it. 2) Keep it out of children’s reach. 3) Don’t keep it in hightemperature or in direct sunlight.

Reported adverse events (FAERS/openFDA)#

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