Olopatadine Hydrochloride Ophthalmic Solution Once Daily

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 Once Daily
Generic name
OLOPATADINE HYDROCHLORIDE OPHTHALMIC
Manufacturer
DOLGENCORP, LLC
Product type
HUMAN OTC DRUG
SPL set ID
fa75f236-0170-e7be-ce8c-7dff7c36fac8
SPL ID
47607abb-5d8a-d789-ee04-1879d00b1897
Version
3
Effective date
2025-12-12
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:12:40
Harmonized routes table
Harmonized routes
OPHTHALMIC

Warnings cross-check#

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warnings

WARNINGS For external use only

Reported adverse events (FAERS/openFDA)#

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