FDA label 4479eba8-0f72-4e9e-83a2-95d351ef2094

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
01cf2af5-6c3d-44cd-ab8d-445bcc5e8afb
SPL ID
4479eba8-0f72-4e9e-83a2-95d351ef2094
Version
1
Effective date
2018-07-24
Source export date
2026-09-28
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/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:13:45

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 Warnings: If you have any of the following problems with cosmetics, you should stop using it. If you continue to use it, your symptoms will worsen. Consult your dermatologist. 1) In case of abnormalities such as red spot, swelling, itching, irritation during use. 2) If the applied area is abnormal due to direct sunlight. Do not use it in areas with scratches, eczema, or dermatitis.

Reported adverse events (FAERS/openFDA)#

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