FDA label 6245b26c-02a7-44b7-af56-985fd2805e53

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
343bb29b-dd47-4d4b-920e-a51034a8fef1
SPL ID
6245b26c-02a7-44b7-af56-985fd2805e53
Version
1
Effective date
2014-01-27
Source export date
2026-10-12
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:06:02

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 1. You can use the cosmetics, if there is an abnormality, such as the following, it is necessary to stop using, because it worsen the symptoms. If you continue to use, that I talk to dermatologists. If there is abnormal red spots, swelling, itching, and irritation to 1) use. When there is an abnormality, such as described above by direct sunlight 2) the application site. 2. That you do not use the site to include a wound, the part with the abnormality of dermatitis and eczema. 3. When it got into eyes, be washed away immediately.

Reported adverse events (FAERS/openFDA)#

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