Label: OLOPATADINE HYDROCHLORIDE solution

  • NDC Code(s): 0363-8022-39, 0363-8022-41
  • Packager: WALGREEN CO.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated November 11, 2021

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  • Drug Facts

    Active ingredient
    Olopatadine (0.2%)
    (equivalent to olopatadine hydrochloride, USP 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 a 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 (1-800-222-1222) 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?

    ✆1-800-925-4733

    Distributed by:
    WALGREEN CO.
    200 WILMOT RD., DEERFIELD, IL 60015

    Made in India

  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL-0.2% (2.5 mL Container)

    Walgreens                NDC 0363-8022-39
    Eye Allergy Itch Relief
    OLOPATADINE HYDROCHLORIDE OPHTHALMIC
    SOLUTION USP, 0.2%
    ANTIHISTAMINE
    Once Daily          2.5 mL (0.085 FL OZ)
    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL-0.2% (2.5 mL Container)

  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL-0.2% (2.5 mL Container Carton)

    ORIGINAL PRESCRIPTION STRENGTH
                                               NDC 0363-8022-39
    Walgreens
    Compare to the active ingredient in
    Pataday® Once Daily Relief‡‡
    Eye Allergy
    Itch Relief
    OLOPATADINE HYDROCHLORIDE
    OPHTHALMIC SOLUTION USP, 0.2%
    ANTIHISTAMINE
    Once Daily
    •  Works in minutes
    •  Relief from allergens:
        pet dander, grass,
        pollen & ragweed
    •  Sterile
    2.5 mL (0.085 FL OZ)


    olopatadine-figure-2
  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL-0.2% (2.5 mL Container Carton) Twin Pack

    TWIN PACK

    ORINIGAL PRESCRIPTION STRENGTH

                                             NDC 0363-8022-41
    Walgreens
    Compare to the active ingredient in
    Pataday® Once Daily Relief‡‡

    Eye Allergy
    Itch Relief
    OLOPATADINE HYDROCHLORIDE
    OPHTHALMIC SOLUTION USP, 0.2%
    ANTIHISTAMINE

    Once Daily
    • Works in minutes
    • Relief from allergens:
       pet dander, grass,
       pollen & ragweed
    • Sterile

    TWO 2.5 mL BOTTLES
    (0.085 FL OZ each)
    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL-0.2% (2.5 mL Container Carton) Twin Pack


  • INGREDIENTS AND APPEARANCE
    OLOPATADINE HYDROCHLORIDE 
    olopatadine hydrochloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-8022
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OLOPATADINE HYDROCHLORIDE (UNII: 2XG66W44KF) (OLOPATADINE - UNII:D27V6190PM) OLOPATADINE HYDROCHLORIDE2 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM (UNII: GR686LBA74)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-8022-391 in 1 CARTON07/15/2020
    12.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:0363-8022-412 in 1 CARTON07/15/2020
    22.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20999507/15/2020
    Labeler - WALGREEN CO. (008965063)
    Registrant - EUGIA Pharma Specialities Limited (650804896)
    Establishment
    NameAddressID/FEIBusiness Operations
    Eugia Pharma Specialities Limited650498244ANALYSIS(0363-8022) , MANUFACTURE(0363-8022)
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