Label: WAL FEX 24 HOUR ALLERGY- fexofenadine hcl tablet, film coated

  • NDC Code(s): 0363-0600-01, 0363-0600-13, 0363-0600-22, 0363-0600-33, view more
    0363-0600-39, 0363-0600-47, 0363-0600-49, 0363-0600-75, 0363-0600-95
  • Packager: Walgreen Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated July 19, 2021

If you are a consumer or patient please visit this version.

  • 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 (1-800-222-1222).

  • 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

    do not use if printed blister unit is broken or torn
    store between 20°-25°C (68°-77°F)
    protect from excessive moisture
    this product meets the requirements of USP Dissolution Test 3
  • Inactive ingredients

    colloidal silicon dioxide, croscarmellose sodium, hypromellose, iron oxide black, iron oxide red, iron oxide yellow, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, titanium dioxide

  • Questions or comments?

    1-800-719-9260

  • Package/Label Principal Display Panel

    NON-DROWSY

    Wal-Fex®

    Compare to Allegra® Allergy active ingredient

    24 HOUR ALLERGY

    FEXOFENADINE HYDROCHLORIDE TABLETS 180 mg / ANTIHISTAMINE

    24 HOUR

    TABLETS

    Indoor/outdoor allergy relief of sneezing; runny nose; itchy, watery eyes & itchy nose or throat

    5 TABLETS

    24 HOUR

    ACTUAL SIZE

    571-94-wal-fex.jpg
  • INGREDIENTS AND APPEARANCE
    WAL FEX 24 HOUR ALLERGY 
    fexofenadine hcl tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0600
    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)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorORANGE (peach) Scoreno score
    ShapeROUNDSize12mm
    FlavorImprint Code 93;7253
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-0600-135 in 1 CARTON03/06/2014
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:0363-0600-2215 in 1 CARTON03/06/2014
    21 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:0363-0600-391 in 1 CARTON03/06/2014
    330 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:0363-0600-951 in 1 CARTON03/06/2014
    445 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:0363-0600-011 in 1 CARTON03/06/2014
    570 in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:0363-0600-751 in 1 CARTON03/06/2014
    690 in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:0363-0600-471 in 1 CARTON03/06/2014
    7150 in 1 BOTTLE; Type 0: Not a Combination Product
    8NDC:0363-0600-331 in 1 CARTON03/06/201403/06/2014
    860 in 1 BOTTLE; Type 0: Not a Combination Product
    9NDC:0363-0600-491 in 1 CARTON03/06/2014
    940 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07644703/06/2014
    Labeler - Walgreen Company (008965063)