FDA label f42b51b2-318e-eb6f-e053-2995a90a56d6

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: 4a721be0-6123-4879-b428-be0a5319e68e
SPL ID: f42b51b2-318e-eb6f-e053-2995a90a56d6
Version: 2
Effective date: 2023-02-08
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:43:23

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		f42b51b2-318e-eb6f-e053-2995a90a56d6	id
spl set id		4a721be0-6123-4879-b428-be0a5319e68e	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 external use only. Do not use this product if • Solution changes color or becomes cloudy When using this product • Remove contact lens before using • To avoid contamination, do not touch tip of container to any surface • Replace cap after using. Keep container tightly closed. 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 Keep out of the reach of children . If accidentally swallowed, get medical help or contact a Poison Control Center.

Reported adverse events (FAERS/openFDA)#

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