WAL FEX 24 HOUR ALLERGY- fexofenadine hcl tablet, film coated 
Walgreen Company

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Walgreen Co. Wal-Fex® 24 Hour Allergy Drug Facts

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
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)

Revised: 7/2021
Document Id: 6f734bfe-aaf9-424c-92ae-a20442628c20
Set id: bb7480e4-4693-4adc-ba74-3c8acf0488d4
Version: 7
Effective Time: 20210719
 
Walgreen Company