Home FDA labels 0dc93b78-bd22-40f7-bfc3-25e1575a197f FDA label 0dc93b78-bd22-40f7-bfc3-25e1575a197f 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 ac26a64a-d59b-424d-8090-091c2cdcc891
SPL ID 0dc93b78-bd22-40f7-bfc3-25e1575a197f
Version 2
Effective date 2019-02-22
Source export date 2026-10-12
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:33:01 Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 2 matching rows.
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: Consult a doctor if rashes, swelling, itching or any other side effects occur due to the direct sunlight during or after using this product. Avoid any wound area. Keep away from reach of children. Keep away from direct sunlight.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.