EYE ITCH RELIEF (KETOTIFEN FUMARATE) SOLUTION/ DROPS [RITE AID CORPORATION]

  • Home
  • EYE ITCH RELIEF (KETOTIFEN FUMARATE) SOLUTION/ DROPS [RITE AID CORPORATION]

EYE ITCH RELIEF (KETOTIFEN FUMARATE) SOLUTION/ DROPS [RITE AID CORPORATION]
PDF | XML
NDC 11822-4201-0
Set ID 7410b0e1-ee10-4ca6-9f36-d84a33619880
Category HUMAN OTC DRUG LABEL
Packager Rite Aid Corporation
Generic Name
Product Class
Product Number
Application Number ANDA077958
View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Ketotifen (0.025%)

    (equivalent to ketotifen fumarate 0.035%)

  • 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
    • replace cap after each use

    Stop use and ask a doctor if you experience any of the following:

    • eye pain
    • changes in vision
    • 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. (1-800-222-1222)

  • Directions

    • Adults and children 3 years of age and older:

      Put 1 drop in the affected eye(s) twice daily, every 8 to 12 hours, no more than twice per day.

    • Children under 3 years of age:

      Consult a doctor.

  • Other information

    • only for use in the eye.
    • store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].
  • Inactive ingredients

    benzalkonium chloride 0.01%, glycerin, Water for Injection. May contain hydrochloric acid and/or sodium hydroxide (to adjust pH).

  • Questions or comments?

    1-800-932-5676

    Serious side effects associated with use of this product may be reported to this number

  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel Text for Container Label:

    Rite Aid Pharmacy Logo®

    ORIGINAL

    PRESCRIPTION STRENGTH

    eye itch relief

    ketotifen fumarate

    ophthalmic solution 0.035%

    antihistamine eye drops

    5 mL (0.17 FL OZ) Sterile

    Principal Display Panel Text for Container Label
  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel Text for Carton Label:

    Rite Aid Pharmacy Logo®

    *Compare to the active

    ingredient of Zaditor®

    ORIGINAL PRESCRIPTION STRENGTH

    eye itch

    relief

    ketotifen fumarate

    ophthalmic solution 0.035%

    antihistamine eye drops

    UP TO 12 HOURS

    ITCH RELIEF

    works in minutes

    for ages 3 years and older

    30-day supply

    Sterile

    5 mL

    (0.17 FL OZ)

    Principal Display Panel Text for Carton Label
  • INGREDIENTS AND APPEARANCE
    EYE ITCH RELIEF 
    ketotifen fumarate solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-4201
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ketotifen fumarate (UNII: HBD503WORO) (ketotifen - UNII:X49220T18G) ketotifen0.35 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    benzalkonium chloride (UNII: F5UM2KM3W7)  
    glycerin (UNII: PDC6A3C0OX)  
    water (UNII: 059QF0KO0R)  
    hydrochloric acid (UNII: QTT17582CB)  
    sodium hydroxide (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-4201-01 in 1 CARTON12/06/2013
    15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07795812/06/2013
    Labeler - Rite Aid Corporation (014578892)
    Registrant - Akorn Operating Company LLC (117693100)
    Establishment
    NameAddressID/FEIBusiness Operations
    Akorn, Inc117696840MANUFACTURE(11822-4201) , ANALYSIS(11822-4201) , STERILIZE(11822-4201) , PACK(11822-4201) , LABEL(11822-4201)
    Establishment
    NameAddressID/FEIBusiness Operations
    Akorn AG482198285MANUFACTURE(11822-4201)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hi-Tech Pharmacal Co. Inc.117696873LABEL(11822-4201) , PACK(11822-4201)
View All Sections

Related Drugs

Search DailyMed Drugs