ALLEGRA ALLERGY- fexofenadine hydrochloride tablet, film coated 
Select Corporation

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Allegra® 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:

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

colloidal silicon dioxide, croscarmellose sodium, hypromellose, iron oxide blends, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, pregelatinized starch, titanium dioxide

Questions or comments?

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

Product Repackaged and Distributed
with permission of manufacturer by:
Select Corporation Carrollton, TX 75007

PRINCIPAL DISPLAY PANEL - 1 Tablet Pouch Blister Pack

Allegra®
ALLERGY
fexofenadine HCl tablet
180 mg/antihistamine
24HR

NON-DROWSY

INDOOR / OUTDOOR
ALLERGY RELIEF

2111920120.A

Sneezing
Runny Nose
Itchy, Watery Eyes
Itchy Nose or Throat

1 TABLET
Actual Size

PRINCIPAL DISPLAY PANEL - 1 Tablet Pouch Blister Pack
ALLEGRA ALLERGY 
fexofenadine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52904-190(NDC:41167-4131)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Fexofenadine hydrochloride (UNII: 2S068B75ZU) (Fexofenadine - UNII:E6582LOH6V) Fexofenadine hydrochloride60 mg
Inactive Ingredients
Ingredient NameStrength
silicon dioxide (UNII: ETJ7Z6XBU4)  
croscarmellose sodium (UNII: M28OL1HH48)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
magnesium stearate (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
polyethylene glycol, unspecified (UNII: 3WJQ0SDW1A)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
titanium dioxide (UNII: 15FIX9V2JP)  
STARCH, CORN (UNII: O8232NY3SJ)  
brown iron oxide (UNII: 1N032N7MFO)  
Product Characteristics
ColorORANGE (peach) Scoreno score
ShapeOVALSize12mm
FlavorImprint Code 06;E
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52904-190-031 in 1 BLISTER PACK12/08/2021
11 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02087212/08/2021
Labeler - Select Corporation (053805599)

Revised: 4/2022
Document Id: c878ce1e-8153-4871-961b-33c8891dcd27
Set id: 78d2742f-250a-4c5c-846f-b45078126281
Version: 1
Effective Time: 20220414
 
Select Corporation