FDA.reportPublic FDA data

FDA label 7f9fcbe8-8a76-5224-e053-2a91aa0a86fc

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
3af13426-4e22-2fb0-e054-00144ff8d46c
SPL ID
7f9fcbe8-8a76-5224-e053-2a91aa0a86fc
Version
2
Effective date
2019-01-16
Source export date
2026-08-17
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-17/0b1cc8680154603ac269ec69e1c6611714d626104ff688eca4b2c067b511bd72/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
ca19d5b1416b6b66a9d383bfdc77d90e91adfeefe16ffcc1ac6b06ceb90d8d73
Import run
20260818T065550Z
Imported at
2026-08-18 07:46:37

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. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms). 1) Occurrence of red spots, swelling, itchiness, and other skin irritation 2) 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. Precaution for Storage and Handling 1) Close the lid after use 2) Keep out of reach of infants and children 3) Do not to store in a place with high/low temperature and exposed to direct sunlight 4. Use as avoiding eye areas.