FDA label 93f938d7-b01f-40b1-980a-01cb1d8aacad

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: 7e005109-cb61-4f18-83f0-7c8447784cfe
SPL ID: 93f938d7-b01f-40b1-980a-01cb1d8aacad
Version: 1
Effective date: 2018-04-12
Source export date: 2026-10-12
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:42:07

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		93f938d7-b01f-40b1-980a-01cb1d8aacad	id
spl set id		7e005109-cb61-4f18-83f0-7c8447784cfe	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 this product changes color or becomes cloudy. if you are sensitive to any ingredient in this product. When using this product avoid contamination, do not touch tip of container to any surface. replace cap after each use. remove contact lenses Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye(s). the condition worsens or persists more than 72 hours. Keep this and all drugs 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.