ALLEGRA ALLERGY- fexofenadine hydrochloride tablet, coated 
Chattem, Inc.

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Allegra Allergy

Allegra Allergy® Gelcaps  24 HOUR

Drug Facts

Active ingredient

(in each tablet)

Fexofenadine HCI 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 overtake one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hours
children under 12 years of agedo not use
adults 65 years of age and olderask a doctor
consumers with kidney diseaseask a doctor

Other information

Inactive ingredients

croscarmellose sodium, D&C red 28, D&C red 33, FD&C blue 1, gelatin, hydroxypropylcellulose, hydroxypropyl methylcellulose, magnesium stearate, microcrystalline cellulose, PEG-135, pharmaceutical ink, pregelatinized starch, titanium dioxide

Questions or comments?

call toll-free 1-800-633-1610 or www.allegra.com 

The makers of Allegra® do not make store brand products. The trade dress of this Allegra® package is subject to trademark protection.
Dist. By: Chattem, Inc., a Sanofi Company, Chattanooga, TN 37409-0219 ©2014

PRINCIPAL DISPLAY PANEL

NDC 41167-4122-0
Allegra® 
ALLERGY
fexofenadine HCI tablet
180 mg/antihistamine
24 HR
8 GELCAPS 

NDC 41167-4122-0
Allegra® 
ALLERGY
fexofenadine HCI tablet
180 mg/antihistamine
24 HR
8 GELCAPS

ALLEGRA ALLERGY 
fexofenadine hydrochloride tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-4122
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
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
D&C RED NO. 28 (UNII: 767IP0Y5NH)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
GELATIN (UNII: 2G86QN327L)  
HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)  
STARCH, CORN (UNII: O8232NY3SJ)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
Colorpurple (White band in the middle) Scoreno score
ShapeOVAL (Caplet) Size20mm
FlavorImprint Code AG;AG
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41167-4122-51 in 1 CARTON12/17/2014
124 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:41167-4122-61 in 1 CARTON12/17/2014
232 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:41167-4122-92 in 1 CARTON12/17/201406/23/2019
3NDC:41167-4122-740 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:41167-4122-21 in 1 CARTON12/17/2014
460 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:41167-4122-01 in 1 CARTON12/17/2014
58 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02087212/17/2014
Labeler - Chattem, Inc. (003336013)

Revised: 8/2021
Document Id: 7b02cf6b-1e6e-429f-997b-991fc71b852e
Set id: f061d6b1-89f7-4d5f-ac59-9c73408517c1
Version: 17
Effective Time: 20210830
 
Chattem, Inc.