Label: WAL-FEX- fexofenadine hydrochloride tablet

  • NDC Code(s): 0363-0784-07, 0363-0784-15, 0363-0784-18, 0363-0784-29, view more
    0363-0784-30, 0363-0784-40, 0363-0784-43, 0363-0784-45, 0363-0784-75, 0363-0784-90
  • Packager: Walgreens Company
  • This is a repackaged label.
  • Source NDC Code(s): 55111-784
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated January 22, 2022

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  • Active ingredient(s)

    Fexofenadine Hydrochloride USP, 180 mg

  • Purpose

    Antihistamine

  • Use(s)

    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

    (blister only) safety sealed: do not use if carton is opened or if individual blister units are torn or opened

    (bottles only) safety sealed: do not use if carton is opened or if printed foil inner seal on bottle is torn or missing

  • Storage

    • 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, powdered cellulose and titanium dioxide

  • Questions?

    Call 1-888-375-3784

  • PRINCIPAL DISPLAY PANEL

    Bottle Carton Label

    15 ct Carton

  • Blister Carton Label: 15 count

    Blister Carton Label

    Carton

  • INGREDIENTS AND APPEARANCE
    WAL-FEX 
    fexofenadine hydrochloride tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0784(NDC:55111-784)
    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:0363-0784-301 in 1 CARTON04/13/2011
    130 in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:0363-0784-432 in 1 CARTON04/13/2011
    230 in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:0363-0784-401 in 1 CARTON04/13/2011
    340 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:0363-0784-451 in 1 CARTON04/13/2011
    445 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:0363-0784-751 in 1 CARTON04/13/2011
    570 in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:0363-0784-151 in 1 CARTON04/13/2011
    6150 in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:0363-0784-901 in 1 CARTON04/13/2011
    790 in 1 BOTTLE; Type 0: Not a Combination Product
    8NDC:0363-0784-071 in 1 CARTON04/13/2011
    85 in 1 BLISTER PACK; Type 0: Not a Combination Product
    9NDC:0363-0784-293 in 1 CARTON04/13/2011
    95 in 1 BLISTER PACK; Type 0: Not a Combination Product
    10NDC:0363-0784-18180 in 1 BOTTLE; Type 0: Not a Combination Product07/13/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07650204/13/2011
    Labeler - Walgreens Company (008965063)
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