ALLERGY RELIEF- fexofenadine hcl tablet, coated 
TARGET Corporation

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DRUG FACTS

Active ingredient (in each film-coated 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 right away.

Directions

adults and children 12 years of age and over

take one 18 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

anhydrous lactose,colloidal silicon dioxide, corn starch, croscarmellose sodium, lactose monohydrate, pregelatinized starch (maize), stearic acid, opadry pink 03B84893 containing hypromellose, polyethylene glycol, red iron oxide, titanium dioxide, and yellow iron oxide

Questions or comments?

call 1-800-910-6874

Principal Display Panel

Compare to the active ingredient in Allegra® Allergy 24 hour*

non-drowsy

Allergy Relief

fexofenadine HCI 180mg / antihistamine

original prescription strength

indoor and outdoor allergies

Relief of:

COATED CAPLETS** (**Capsule-shaped tablets)

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

TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING.

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.

Distributed by Target Corporation

Minneapolis, MN 55403

TM & ©2018 Target Brands, Inc.

Product Label

Fexofenadine HCI USP 180 mg

TARGET Non-Drowsy Allergy Relief

ALLERGY RELIEF 
fexofenadine hcl tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-104
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)  
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
ColorwhiteScoreno score
ShapeCAPSULESize17mm
FlavorImprint Code SG;202
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-104-151 in 1 CARTON01/11/201805/30/2025
115 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:11673-104-121 in 1 BOX01/11/201805/30/2025
2120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:11673-104-701 in 1 BOX01/11/201805/30/2025
370 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4NDC:11673-104-301 in 1 BOX01/11/201805/30/2025
440 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07911201/11/201805/30/2025
Labeler - TARGET Corporation (006961700)

Revised: 11/2023
Document Id: c90451f9-0f9f-4fd7-af22-5f2f544f089e
Set id: 9a36d049-6ff8-4d78-bb89-8281f3266fd5
Version: 6
Effective Time: 20231101
 
TARGET Corporation