Home FDA labels 0038f516-ca67-3338-e063-6394a90a250c FDA label 0038f516-ca67-3338-e063-6394a90a250c 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 c62b66b2-8a59-3a28-e053-2a95a90aa06b
SPL ID 0038f516-ca67-3338-e063-6394a90a250c
Version 2
Effective date 2023-07-11
Source export date 2026-10-30
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run 20261102T182004Z
Imported at 2026-11-02 18:34:02 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. ■ Do not use on eyes. If eye contact occurs, rinse eyes thoroughly with water. ■ Do not flush.■ Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.