FDA.reportPublic FDA data

FDA label ba50ef43-cd6d-4a2c-b1b0-dd1b741d5a75

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
3590c846-0779-4ed8-9d25-a15890faa24a
SPL ID
ba50ef43-cd6d-4a2c-b1b0-dd1b741d5a75
Version
2
Effective date
2021-07-12
Source export date
2026-10-12
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/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:41:09

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: For external use only In case of having following symptoms after using this, you are advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist In case of having problems such as red rash, swollenness, itching, stimulation during usage Do not use it open wounds that are prone to infection Precautious for handling and storage Keep it away from young children or infants Keep it out of the direct sunlight

Reported adverse events (FAERS/openFDA)#

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