FDA label a7489118-9d71-4ad8-a5a8-f04410fc63ed

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: 79dc1d94-310e-4a5c-bbd4-b61fc506dc34
SPL ID: a7489118-9d71-4ad8-a5a8-f04410fc63ed
Version: 13
Effective date: 2011-01-25
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 01:42:02

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		a7489118-9d71-4ad8-a5a8-f04410fc63ed	id
spl set id		79dc1d94-310e-4a5c-bbd4-b61fc506dc34	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: To be used for cataract when a diagnosis has been made by a physician. For external use only. Initial exacerbation of symptoms may occur. Use only if bottle seal is intact. To avoid contamination, do not touch the tip of the container to any surface. Use within 30 days of opening. Expiration date only refers to unopened bottle. Replace cap tightly after every use. Contact wearers: consult physician prior to using. Keep this and all medicines out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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