FDA label f2eb3005-b0e4-4404-bf97-0a1c9910e5b5

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: c26707f1-2e60-4387-890d-99e2254e7310
SPL ID: f2eb3005-b0e4-4404-bf97-0a1c9910e5b5
Version: 1
Effective date: 2018-01-19
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 02:48:16

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.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		f2eb3005-b0e4-4404-bf97-0a1c9910e5b5	id
spl set id		c26707f1-2e60-4387-890d-99e2254e7310	set_id

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 use in the eye s only. ● Retain outer carton for full product drug facts Do not use ● If solution changes color, or becomes cloudy. When using this product ● avoid contamination, do not touch tip of container to any surface. ● replace cap after each use. Stop use and ask a doctor i f ● you experience eye pain, changes in vision, continued redness or irritation of the eye(s) ● the condition worsens or persists for more than 72 hours. Keep out of the reach of children . If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Reported adverse events (FAERS/openFDA)#

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