FDA.reportPublic FDA data

FDA label ba173b5f-dc77-a9e3-e053-2995a90ad74a

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
ba173b5f-dc76-a9e3-e053-2995a90ad74a
SPL ID
ba173b5f-dc77-a9e3-e053-2995a90ad74a
Version
1
Effective date
2021-01-29
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:16:10

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.