Label: EYE ALLERGY ITCH RELIEF- olopatadine hcl solution/ drops

  • NDC Code(s): 70000-0053-1
  • Packager: CARDINAL HEALTH 110, LLC. DBA LEADER
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated February 13, 2026

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  • ACTIVE INGREDIENT

    Olopatadine (0.2%)  (equivalent to olopatadine hydrochloride 0.222%)

  • PURPOSE

    Antihistamine

  • USE

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

  • 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
  • STOP USE AND ASK DOCTOR IF

    you experience:  

    • eye pain
    • changes in vision
    • increased redness of the eye
    • itching worsens or lasts for more than 72 hours
  • 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:
    • put 1 drop in the affected eye(s) once daily, no more than once 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
  • OTHER INFORMATION

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

  • 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?

    Call 1-888-375-3784

  • SPL UNCLASSIFIED SECTION

    DISTRIBUTED BY:

    CARDINAL HEALTH

    DUBLIN, OHIO 43017

    www.myleader.com

    1-800-200-6313

    Made in India

    Code: AP/DRUGS/103/97

    Rev. 11/25

    CIN 5659222

    ©2025 CARDINAL HEALTH, LEADER, and LOGOs are trademarks of Cardinal Health. All other marks are the property of their respective owners.

    *This product is not manufactured or distributed by Alcon Laboratories Inc., distributor of Pataday® Once Daily Relief. Pataday® is a registered trademark of Novartis AG.

    100% Money Back Guarantee

    Return to place of purchase if not satisfied.

  • PRINCIPAL DISPLAY PANEL

    Carton Label:

    NDC 70000-0053-1

    Original Prescription Strength

    Eye Allergy Itch Relief

    Olopatadine HCl Opthalmic Solution USP, 0.2%

    Antihistamine

    Once Daily Relief

    Works in Minutes

    Once Daily

    Sterile

    2.5 mL (0.085 fl oz)

    For Ages 2 and Older

    30 DAY SUPPLY

    TAMPER EVIDENT: Packaged with Tamper-Evident bottle cap. Do Not Use if breakable ring is separated or missing.

    COMPARE TO PATADAY® ONCE DAILY RELIEF active ingredient*

    Carton

    Container Label:

    NDC 70000-0053-1

    Eye Allergy Itch Relief

    Olopatadine Hydrochloride

    Ophthalmic Solution USP, 0.2%

    Antihistamine

    ONCE DAILY RELIEF

    Sterile

    2.5 mL (0.085 fl oz)

    Container
  • INGREDIENTS AND APPEARANCE
    EYE ALLERGY ITCH RELIEF 
    olopatadine hcl solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70000-0053
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OLOPATADINE HYDROCHLORIDE (UNII: 2XG66W44KF) (OLOPATADINE - UNII:D27V6190PM) OLOPATADINE2 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    POVIDONE K30 (UNII: U725QWY32X)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70000-0053-11 in 1 CARTON01/15/2021
    12.5 mL in 1 BOTTLE, DROPPER; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20975201/15/2021
    Labeler - CARDINAL HEALTH 110, LLC. DBA LEADER (063997360)
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