FDA label 04e82b16-1c6e-45f8-b596-381e5dbcbea5

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
04e82b16-1c6e-45f8-b596-381e5dbcbea5
SPL ID
04e82b16-1c6e-45f8-b596-381e5dbcbea5
Version
1
Effective date
2013-07-11
Source export date
2026-11-06
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/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:28:14

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.