FDA.reportPublic FDA data

FDA label ba7c6904-1879-3dd4-e053-2995a90a0405

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
b9ee9390-2e66-84e8-e053-2995a90a9c26
SPL ID
ba7c6904-1879-3dd4-e053-2995a90a0405
Version
5
Effective date
2021-01-01
Source export date
2026-10-30
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:32:09

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

1. If any of the following Symptoms occur, Cease use immediately. Continued usage would exacerbate the symptoms. If symptoms persist, consult a doctor. 1) During of after usage, if red spots appear or you suffer from welling or itching or any other abnormal symptoms after direct exposure to sunlight, consult a doctor immediately. 2)Avoid usage on cuts and wounds. 3) Storage and usage precautions. A) Keep it out of reach of children. B) Avoid exposure to direct sunlight during storage.

Reported adverse events (FAERS/openFDA)#

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