Official product label reference

Olopatadine Hydrochloride — YYBA CORP

This page contains 12 source sections for OLOPATADINE HYDROCHLORIDE, ophthalmic route. Label set 598156e4-f183-86f5-e063-6294a90a64df, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Use temporarily relieves itchy eyes due to pollen, ragweed, grass, animal hair and dander

Purpose

Purpose Antihistamine

Dosage and administration — label text

Directions adults and children 2 years of age and older: put 1 drop in the affected eye(s) once daily, no more than once per day if using other opthalmic products while using this product, wait at least 5 minutes between each product replace cap after each use childrent under 2 yeats of age: consult a doctor

Warnings

Warnings For external use only

Active ingredient

Active ingredient Olopatadine (0.2%) (equivalent to olopatadine hydrochloride, USP 0.222%)

Do not use

Do not use if solution changes color or becomes cloudy if you are sensitive to any ingredient in this product to treat contact lens related irritation

While using this medicine

When using this product do not touch tip of container to any surface to avoid contamination remove contact lenses before use wait at least 10 minutes before reinsterting contact lenses after use do not wear a contact lens if your eye is red

When to stop use and seek help

Stop use and ask a doctor if you experience: Stop use and ask a doctor if: eye pain changes in vision increased redness of the eye itching worsens or lasts for more than 72 hours

Child safety

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Other safety information

Other information only for use in the eye store between 2 degrees to 25 degrees celsius (36 degrees to 77 degrees farenheit)

Inactive ingredient

Inactive ingredients benzalkonium chloride 0.01%, dibasic sodium phosphate, edetate disodium, hydrochloric acid/sodium hydroxide (adjust pH), povidone, sodium chloride and water for injection

Questions

Questions? 1-866-933-6337

Official sources and product identifiers

DailyMed — complete source labelVerify the current version and original formatting, including tables and diagrams.
openFDA — structured source recordMachine-readable label source, linked by the exact label set ID.
Drugs@FDA application ANDA204812Application history where available; verify the specific product and indication.

Substances listed: OLOPATADINE HYDROCHLORIDE

RxNorm identifiers: 1111343

Package NDC codes

73581-712-02

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.

Olopatadine Hydrochloride drug information