OTC Medication Information: Wal Fex 24 Hour Allergy

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

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

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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

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(click image for full-size original)
WAL FEX 24 HOUR ALLERGY
fexofenadine hcl tablet, film coated
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0600
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FEXOFENADINE HYDROCHLORIDE (FEXOFENADINE) FEXOFENADINE HYDROCHLORIDE 180 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
CROSCARMELLOSE SODIUM
HYPROMELLOSE, UNSPECIFIED
FERROSOFERRIC OXIDE
FERRIC OXIDE RED
FERRIC OXIDE YELLOW
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
POLYETHYLENE GLYCOL, UNSPECIFIED
POVIDONE, UNSPECIFIED
TITANIUM DIOXIDE
Product Characteristics
Color ORANGE (peach) Score no score
Shape ROUND Size 12mm
Flavor Imprint Code 93;7253
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0363-0600-13 5 BLISTER PACK in 1 CARTON contains a BLISTER PACK
1 1 TABLET, FILM COATED in 1 BLISTER PACK This package is contained within the CARTON (0363-0600-13)
2 NDC:0363-0600-22 15 BLISTER PACK in 1 CARTON contains a BLISTER PACK
2 1 TABLET, FILM COATED in 1 BLISTER PACK This package is contained within the CARTON (0363-0600-22)
3 NDC:0363-0600-39 1 BOTTLE in 1 CARTON contains a BOTTLE
3 30 TABLET, FILM COATED in 1 BOTTLE This package is contained within the CARTON (0363-0600-39)
4 NDC:0363-0600-95 1 BOTTLE in 1 CARTON contains a BOTTLE
4 45 TABLET, FILM COATED in 1 BOTTLE This package is contained within the CARTON (0363-0600-95)
5 NDC:0363-0600-01 1 BOTTLE in 1 CARTON contains a BOTTLE
5 70 TABLET, FILM COATED in 1 BOTTLE This package is contained within the CARTON (0363-0600-01)
6 NDC:0363-0600-75 1 BOTTLE in 1 CARTON contains a BOTTLE
6 90 TABLET, FILM COATED in 1 BOTTLE This package is contained within the CARTON (0363-0600-75)
7 NDC:0363-0600-47 1 BOTTLE in 1 CARTON contains a BOTTLE
7 150 TABLET, FILM COATED in 1 BOTTLE This package is contained within the CARTON (0363-0600-47)
8 NDC:0363-0600-33 1 BOTTLE in 1 CARTON contains a BOTTLE
8 60 TABLET, FILM COATED in 1 BOTTLE This package is contained within the CARTON (0363-0600-33)
9 NDC:0363-0600-49 1 BOTTLE in 1 CARTON contains a BOTTLE
9 40 TABLET, FILM COATED in 1 BOTTLE This package is contained within the CARTON (0363-0600-49)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076447 03/06/2014
Labeler — Walgreen Company (008965063)

Revised: 02/2020 Walgreen Company

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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