Olopatadine Hydrochloride Ophthalmic Solution

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)

Brand name
Olopatadine Hydrochloride Ophthalmic Solution
Generic name
OLOPATADINE HYDROCHLORIDE OPHTHALMIC
Manufacturer
Albertsons Companies
Product type
HUMAN OTC DRUG
SPL set ID
685192af-d729-3066-5825-6d0e03ce787e
SPL ID
ac0a51c9-185a-9d58-cb21-ee5b6a1134d6
Version
5
Effective date
2025-12-12
Source export date
2026-10-12
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:54:44
Harmonized routes table
Harmonized routes
OPHTHALMIC

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS For external use only

Reported adverse events (FAERS/openFDA)#

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