FDA.reportPublic FDA data

FDA label 245220e7-cc83-4f8f-a01b-acf72e6c59c1

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
01c82eea-de63-4e92-a62e-88fcf0108875
SPL ID
245220e7-cc83-4f8f-a01b-acf72e6c59c1
Version
1
Effective date
2016-10-05
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 05:13:35

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: 1. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms): a) Red spots, swelling, itchiness, and other skin irritation b) If the symptoms above occur after the application area is exposed to direct sunlight. 2. Do not use on open wounds, eczema, and other skin irritations. 3. Storing and handling a) Close the lid after every use. b) Keep out of reach of infants and children. c) Do not store at extreme temperatures or in an area exposed to direct sunlight. 4. Wash away immediately when permeating into the eyes.

Reported adverse events (FAERS/openFDA)#

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