FDA label a4eb5207-f3c5-42cd-978d-6527f8b556bb

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
93f5c5c2-8f66-48dc-a569-0fb5433a8ee3
SPL ID
a4eb5207-f3c5-42cd-978d-6527f8b556bb
Version
1
Effective date
2013-07-08
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 01:25:30

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

■ discontinue use if the following abnormal situations occur If you continue to use, ti may worsen symptoms, consult a dermatologist etc - if signs of redness, skin swelling, itchy spots, irritation or rash etc appear - if above signs appear in the applied area by direct rays of the sun ■ do not use over wounds, rashes, inflammantions or other troubled areas ■ make sure to leave the skin over your eyes uncovered by the facial mask Other Information ■ keep closing the cap after use ■ keep out of reach of children ■ do not keep in the place of high or low temperature and in direct sunlight

Reported adverse events (FAERS/openFDA)#

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