ALLERGY RELIEF- fexofenadine hcl tablet, coated 
Walgreens

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DRUG FACTS

Active ingredient (in each tablet)

Fexofenadine HCl USP, 180 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

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 (1-800-222-1222) 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


Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, hypromellose, iron oxide black, iron oxide red, iron oxide yellow, lactose monohydrate, magnesium stearate, microcrystalline cellulose pregelatinized starch (maize), polyethylene glycol, titanium dioxide

Questions or comments?

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

Principal Display Panel

Compare to the active ingredient in Allegra® Allergy 24 HR††

NON-DROWSY

Allergy Relief

24 HOUR ALLERGY

FEXOFENADINE HCI TABLETS 180mg / ANTIHISTAMINE

24 HOUR  Indoor & Outdoor Allergies

CAPLETS**

(**capsule-shaped tablets)

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

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

Product Label

Fexofenadine HCl USP, 180 mg

WALGREENS Allergy Relief

ALLERGY RELIEF 
fexofenadine hcl tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-8010
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)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
STARCH, CORN (UNII: O8232NY3SJ)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
Product Characteristics
Colorwhite (Peach) Scoreno score
ShapeCAPSULESize17mm
FlavorImprint Code G6
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-8010-1515 in 1 CARTON09/17/2021
11 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:0363-8010-701 in 1 BOX09/17/2021
270 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:0363-8010-451 in 1 BOX09/17/2021
345 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4NDC:0363-8010-301 in 1 BOX09/17/2021
430 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
5NDC:0363-8010-055 in 1 CARTON09/17/2021
51 in 1 BLISTER PACK; Type 0: Not a Combination Product
6NDC:0363-8010-901 in 1 BOX09/17/2021
690 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21107509/17/2021
Labeler - Walgreens (008965063)

Revised: 6/2023
Document Id: 333707e7-77d5-4836-a77c-92f23f6fb85c
Set id: f87455f4-25a1-4882-82b0-e1b5554045a1
Version: 5
Effective Time: 20230613
 
Walgreens