FDA.reportPublic FDA data

FDA label 8041bbe5-8aa2-0905-e053-2991aa0a4805

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
8041bbe5-8aa1-0905-e053-2991aa0a4805
SPL ID
8041bbe5-8aa2-0905-e053-2991aa0a4805
Version
1
Effective date
2019-01-24
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:29:44

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 of the product if any of the following symptoms occurred. Consult a dermatologist if the symptoms got worse. a) If redness, Swelling, Itchiness, Irritation occurred during using. b) If the above symptoms started to occur when exposed to direct sunlight. Do not use on skins with wounds, eczema or dermatitis. Storage instructions a) Always close the lid after finish using. b) Store in a safe place away and out of reach of children. c) Store in a place with not too high or low temperature, keep awayfrom direct sunlight exposure.

Reported adverse events (FAERS/openFDA)#

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