FDA label e21ee458-6cb6-4fcc-948c-0d059f1975d7

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
5b110cd3-abe4-424d-aa9b-81216670d202
SPL ID
e21ee458-6cb6-4fcc-948c-0d059f1975d7
Version
1
Effective date
2018-07-24
Source export date
2026-10-12
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:26:30

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: If you have any of the following problems with cosmetics, you should stop using it. If you continue to use it, your symptoms will worsen. Consult your dermatologist. 1) In case of abnormalities such as red spot, swelling, itching, irritation during use. 2) If the applied area is abnormal due to direct sunlight. Do not use it in areas with scratches, eczema, or dermatitis.

Reported adverse events (FAERS/openFDA)#

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