FDA label 35576ab9-9ec7-42bf-83a9-5f5d6d0c5c1c

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
ac1ea23c-f1c6-418f-921e-58553ee919cb
SPL ID
35576ab9-9ec7-42bf-83a9-5f5d6d0c5c1c
Version
3
Effective date
2024-01-18
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:39:02

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 this product if solution changes color or becomes cloudy Stop use and ask a doctor if you experience • eye pain • changes in vision • continued redness or irritation of the eye or if the condition worsens or persists for more than 72 hours When using this product • to avoid contamination do not touch tip of container to any surface • replace cap after using. Keep container tightly closed. • remove contact lens before using Keep out of the reach children. If accidentally swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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