FDA.reportPublic FDA data

FDA label 5f01e8c7-54d0-42f9-8768-6ee44058148c

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
e43d8c0f-3fda-4d1f-8b2f-3e2565a5a55d
SPL ID
5f01e8c7-54d0-42f9-8768-6ee44058148c
Version
1
Effective date
2019-05-08
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 01:52:06

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 Precautions of Use - In case of contact with eyes, wash immediately - If you do not rinse thoroughly after use, it may cause hair loss or discoloration, so please rinse thoroughly with clean water. - Please do not use the area where there is a wound or eczema and dermatitis. - Stop using and see a doctor 1) If you have abnormalities such as red spots, swelling, itching, irritation during use 2) If there is any abnormality such as above due to direct sunlight

Reported adverse events (FAERS/openFDA)#

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