FDA label 19400574-c997-475d-b454-a1d3a213948d

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: c7acc338-2b84-4929-9b23-3abc35a3edcd
SPL ID: 19400574-c997-475d-b454-a1d3a213948d
Version: 4
Effective date: 2022-01-27
Source export date: 2026-09-28
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:13:55

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		19400574-c997-475d-b454-a1d3a213948d	id
spl set id		c7acc338-2b84-4929-9b23-3abc35a3edcd	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 Do not use this product except under the advice and supervision of a doctor. if imprinted seal is broken or missing. if solution changes color or becomes cloudy. When using this product temporary burning and irritation upon being instilled into eye may occur. to avoid contamination, do not touch tip of container to any surface. replace cap after each use. Stop use and ask a doctor if you experience eye pain. you experience changes in vision. redness or irritation of the eye continues condition worsens or persists. Keep out of reach of children. If 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.