FDA.reportPublic FDA data

FDA label ba3f0442-f3a8-6e3f-e053-2a95a90af13a

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
ba3f0442-f3a7-6e3f-e053-2a95a90af13a
SPL ID
ba3f0442-f3a8-6e3f-e053-2a95a90af13a
Version
1
Effective date
2021-01-31
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:52:41

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.