Label: ALLERGY RELIEF- fexofenadine hydrochloride tablet

  • NDC Code(s): 46122-462-22, 46122-462-61, 46122-462-65, 46122-462-75
  • Packager: AMERISOURCEBERGEN DRUG CORPORATION
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated August 15, 2022

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  • Active ingredient (in each tablet)

    Fexofenadine HCl USP, 180 mg

  • Purpose

    Antihistamine

  • Uses

    temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

    • runny nose
    • itchy, watery eyes
    • sneezing
    • itching of the nose or throat



  • Warnings

    Do not use

    if you have ever had an allergic reaction to this product or any of its ingredients.

    Ask a doctor before use if you have

    kidney disease. Your doctor should determine if you need a different dose.

    When using this product

    • do not take more than directed
    • do not take at the same time as aluminum or magnesium antacids
    • do not take with fruit juices (see Directions)

    Stop use and ask doctor if

    an allergic reaction to this product occurs. Seek medical help right away.

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

    In case of  overdose, get medical help or contact a Poison Control Center right away.

  • Directions

    adults and children 12 years of age and over         take one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hours
    children under 12 years of agedo not use
    adults 65 years of age  and olderask a doctor
    consumers with kidney diseaseask a doctor
  • Other information

    • safety sealed: do not use if carton is opened or if printed foil inner seal on bottle is torn or missing
    • store between 20 and 25°C (68 and 77°F)
    • protect from excessive moisture
    • this product meets the requirements of USP Dissolution Test 2

  • Inactive ingredients

    colloidal silicon dioxide, corn starch, croscarmellose sodium, FD&C Red no. 40, hypromellose, iron oxide black, magnesium stearate, mannitol, polyethylene glycol, powder cellulose, and titantium dioxide

  • Questions?

    call 1-888-375-3784

  • Package Label - 90 Count Carton

    Good Neighbor Pharmacy®

    Compare to the active ingredient in Allegra® Allergy 24 Hour Tablets*

    NDC 46122-462-75

    Allergy Relief
    fexodenadine hydrochloride
    tablets, 180 mg
    Antihistamine

    Relief of:

    • Sneezine
    • Runny Nose
    • Itchy, Watery Eyes
    • Itchy Nose or Throat

    Indoor and Outdoor
    Allergies

    Non-Drowsy

    24
    HOUR

    carton

  • Package Label - 90 Count Label

    Good Neighbor Pharmacy®

    NDC 46122-462-75

    Allergy Relief  
    fexodenadine hydrochloride tablets,
    180 mg  
    Antihistamine
    24-Hour

    Indoor and Outdoor Allergies Non-Drowsy

    container

  • INGREDIENTS AND APPEARANCE
    ALLERGY RELIEF 
    fexofenadine hydrochloride tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-462
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Fexofenadine Hydrochloride (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V) Fexofenadine Hydrochloride180 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    magnesium stearate (UNII: 70097M6I30)  
    mannitol (UNII: 3OWL53L36A)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    polyethylene glycol 400 (UNII: B697894SGQ)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    Product Characteristics
    ColorPINKScoreno score
    ShapeOVALSize7mm
    FlavorImprint Code 194;R
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:46122-462-651 in 1 CARTON02/20/2018
    130 in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:46122-462-223 in 1 CARTON02/20/2018
    25 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:46122-462-611 in 1 CARTON02/20/2018
    345 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:46122-462-751 in 1 CARTON02/20/2018
    490 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07650202/20/2018
    Labeler - AMERISOURCEBERGEN DRUG CORPORATION (007914906)
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