FDA label 927d3dc1-d4f8-41c6-95fe-5fa83588fcff

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
cd521887-2c6e-428f-8e86-08ab9338ce2b
SPL ID
927d3dc1-d4f8-41c6-95fe-5fa83588fcff
Version
1
Effective date
2013-07-11
Source export date
2026-11-06
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/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:43:12

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.