Home FDA labels cfda7dff-ac10-06da-e053-2995a90ad541 FDA label cfda7dff-ac10-06da-e053-2995a90ad541 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 a79f0197-0fd7-5520-e053-2a95a90ab093
SPL ID cfda7dff-ac10-06da-e053-2995a90ad541
Version 2
Effective date 2021-11-02
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/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run 20261108T063105Z
Imported at 2026-11-08 07:50:25 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 For external use only. Do not use: In the eyes. If you are allergic to any of the ingredients. When using the product if eye contact occours, rinse thoroughly with water. Stop and ask a doctor if irritation and redness develops and presists for more than 72 hours.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.