Olopatadine Hydrochloride OLOPATADINE HYDROCHLORIDE TARGET CORPORATION FDA Approved Uses temporarily relieves itchy and red eyes due to pollen, ragweed, grass, animal hair and dander
FunFoxMeds box
Route
OPHTHALMIC
Applications
ANDA206046
Package NDC

Drug Facts

Composition & Profile

Active Ingredients
Active ingredient Olopatadine (0.1%) (equivalent to olopatadine hydrochloride 0.111%)
Inactive Ingredients
Inactive ingredients benzalkonium chloride 0.01% dibasic sodium phosphate hydrochloric acid/sodium hydroxide (to adjust pH) sodium chloride and water for injection
Treats Conditions
Uses Temporarily Relieves Itchy And Red Eyes Due To Pollen Ragweed Grass Animal Hair And Dander

Identifiers & Packaging

Container Type BOX
All Product Codes
UNII
2XG66W44KF
Packaging

Package/Label Principal Display Panel TARGET CARTON

Package Descriptions
  • Package/Label Principal Display Panel TARGET CARTON

Overview

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

Indications & Usage

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

Dosage & Administration

Directions adults and children 2 years of age and older: put 1 drop in the affected eye(s) twice daily, every 6 to 8 hours, no more than twice per day if using other ophthalmic products while using this product, wait at least 5 minutes between each product replace cap after each use children under 2 years of age: consult a doctor

Warnings & Precautions
Warnings For external use only
Purpose

Purpose Antihistamine and Redness Reliever

Keep Out of Reach of Children

Keep Out of Reach of Children. If swallowed, get medical help or contact a Poison Control Center right away.

Questions

Questions? Call 1-800-910-6874


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