Home > Drugs A-Z > Fexofenadine HCl

Fexofenadine HCl (Chain Drug Consortium, LLC (Premier Value))

Available Formats

Dosage Form Package Information Links
TABLET 1 BOTTLE in 1 BOX (68016-119-00) > 30 TABLET in 1 BOTTLE Label Information
TABLET 1 BOTTLE in 1 BOX (68016-119-01) > 45 TABLET in 1 BOTTLE Label Information

Complete Fexofenadine HCl Information

  • Active ingredient (in each tablet)

    Fexofenadine HCl 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 a 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 age  do not use
     adults 65 years of age and older  ask a doctor
     consumers with kidney disease  ask a doctor

  • Other information

    • store at 20°-25°C (68°-77°F)
    • protect from excessive moisture

  • Inactive ingredients

    colloidal silicon dioxide, croscarmellose sodium, hypromellose, iron oxide red, iron oxide yellow, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone k-30, talc, titanium dioxide.


  • Questions or comments?

    call toll free 1-877-753-3935 Monday- Friday 9AM- 5PM EST


  • Package/Label Principal Display Panel

    *Compare to the active ingredient in Allegra® Allergy 24 hour

    ORIGINAL PRESCRIPTION STRENGTH

    NON-DROWSY

    Fexofenadine HCl Tablets, USP

    180 mg/ ANTIHISTAMINE    

    ALLERGY

    INDOOR & OUTDOOR ALLERGIES

    24 Hour Relief of:

    • sneezing
    • runny nose
    • itchy, watery eyes
    • itchy nose or throat

    *This product is not manufactured or distributed by Chattem Inc., distributor of Allegra® Allergy 24 hour

    KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.

    SAFETY SEALED: DO NOT USE IF CARTON IS OPEN OR IF INNER SEAL IMPRINTED WITH "SEALED FOR YOUR PROTECTION" IS MISSING OR TORN

    Distributed by: CHAIN DRUG CONSORTIUM, LLC.

    3301 NW BOCA RATON BLVD. SUITE 101

    BOCA RATON, FL 33431


  • Product Label

    Premier Value fexofenadine HCl

    Fexofenadine HCl 180 mg


  • INGREDIENTS AND APPEARANCE
    FEXOFENADINE HCL 
    fexofenadine hcl tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:68016-119
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V) FEXOFENADINE HYDROCHLORIDE 180 mg
    Inactive Ingredients
    Ingredient Name Strength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    POVIDONES (UNII: FZ989GH94E)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Color WHITE (Light peach) Score no score
    Shape CAPSULE Size 17mm
    Flavor Imprint Code W987
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68016-119-00 1 in 1 BOX
    1 30 in 1 BOTTLE; Type 0: Not a Combination Product
    2 NDC:68016-119-01 1 in 1 BOX
    2 45 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA079112 06/18/2012
    Labeler - Chain Drug Consortium, LLC (101668460)