Home FDA labels 29e4f451-a6c4-c708-e063-6294a90a4649 FDA label 29e4f451-a6c4-c708-e063-6294a90a4649 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 e37b225d-c7f7-111e-e053-2995a90a72b8
SPL ID 29e4f451-a6c4-c708-e063-6294a90a4649
Version 7
Effective date 2024-12-22
Source export date 2026-11-06
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/2026-11-06/3b52cde3709f43d454872fcaffdb78395b270bc65272c06ef1005cc77c998864/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run 20261106T075659Z
Imported at 2026-11-06 09:00:28 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 For External Use Only When using this product do not use near eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if condition worsens. symptoms may last more than 7 days or clear up and occur again within a few days
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.