FDA label ae69f978-baed-4a37-b6aa-3eb54ce07dd0

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
22774ed4-c620-4f2c-8116-d50dad5ec6b7
SPL ID
ae69f978-baed-4a37-b6aa-3eb54ce07dd0
Version
1
Effective date
2013-01-30
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:21:57

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

1.Avoid using on blemishes, pimples, irritated or sunburned skin. 2. Stop using if skin becomes red, swollen, and itchy during and after use. 3. If pain persists after make is peeled off and above sings occur, discontinue immediately and consult your doctor. 4. Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

Reported adverse events (FAERS/openFDA)#

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