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  5. Label Information: Olopatadine Hydrochloride

FDA Label for Olopatadine Hydrochloride

View Indications, Usage & Precautions

Table of Contents

    1. OTC - PURPOSE
    2. INDICATIONS & USAGE
    3. WARNINGS
    4. DO NOT USE
    5. WHEN USING THIS PRODUCT
    6. OTC - STOP USE
    7. OTC - KEEP OUT OF REACH OF CHILDREN
    8. DIRECTIONS
    9. OTHER INFORMATION
    10. INACTIVE INGREDIENTS
    11. QUESTIONS?
    12. PRINCIPAL DISPLAY PANEL

Olopatadine Hydrochloride Product Label

The following document was submitted to the FDA by the labeler of this product Glenmark Therapeutics Inc., Usa. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Otc - Purpose



Purpose

Active Ingredients

 

Olopatadine 0.2%
(equivalent to olopatadine hydrochloride 0.222%)

Antihistamine


Indications & Usage



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


Warnings



Warnings
For external use only


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

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 reinserting contact lenses after use
  • •do not wear a contact lens if your eye is red

Otc - Stop Use



Stop use and ask a doctor if you experience:

  • •eye pain
  • •changes in vision
  • •increased redness of the eye
  • •itching worsens or lasts for more than 72 hours

Otc - 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.


Directions



  • •adults and children 2 years of age and older:
    • oput 1 drop in the affected eye(s) once daily, no more than once per day
    • oif using other ophthalmic products while using this product, wait at least 5 minutes between each product
    • oreplace cap after each use
    • •children under 2 years of age: consult a doctor

Other Information



  • •only for use in the eye
  • •store between 2°C to 25°C (36°F to 77°F)

Inactive Ingredients



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


Questions?



In the U.S., call toll free weekdays 9 AM to 6 PM EST at 1 (888) 721-7115.

Distributed by:

Glenmark Therapeutics Inc., USA

Mahwah, NJ 07430

March 2025


Principal Display Panel



Olopatadine hydrochloride 
ophthalmic solution 0.2% 

Antihistamine
2.5 mL
STERILE

EYE ALLERGY ITCH RELIEF

label - label

label - label

Original Prescription Strength

ONCE DAILY RELIEF

Olopatadine hydrochloride ophthalmic solution 0.2%
Antihistamine
Eye Allergy Itch Relief

STERILE
2.5 mL

NDC: 72657-194-25


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