FDA label 3731f315-4cba-83e9-e063-6294a90aba6a

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
322a3670-e9b1-9734-e063-6394a90a00bd
SPL ID
3731f315-4cba-83e9-e063-6294a90aba6a
Version
2
Effective date
2025-06-10
Source export date
2026-09-28
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:04:47

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. Consult a specialist if you have abnormal symptoms or side effects such as red spots, swelling, or itching due to direct sunlight during or after using this product. 2. Please refrain from using the wound area 3. Precautions for Storage and Handling A. Please keep it out of the reach of children. B. Please store it in a cool place. 4. Wash it immediately when it gets into your eyes.

Reported adverse events (FAERS/openFDA)#

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