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Allegra Allergy Prescribing Information

Package insert / product label
Generic name: fexofenadine hydrochloride
Dosage form: tablet, film coated
Drug class: Antihistamines

Medically reviewed by Drugs.com. Last updated on Apr 16, 2024.

Allegra Allergy

Allegra Allergy® - 12/24 HOUR

Drug Facts

Active ingredient

(in each tablet)
12 Hour Tablet: Fexofenadine HCl 60 mg

24 Hour Tablet: Fexofenadine HCl 180 mg

Purpose

Antihistamine

Indications and Usage for Allegra Allergy

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

  • runny nose
  • sneezing
  • itchy, water eyes
  • 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.

Allegra Allergy Dosage and Administration

adults and children 12 years of age and overtake one 60 mg tablet with water every 12 hours; do not take
more than 2 tablets 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

Allegra Allergy Dosage and Administration

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

  • safety sealed: do not use if carton is opened or if individual blister units are torn or opened or if inner foil seal on bottle is torn or missing
  • store between 20° and 25°C (68° and 77°F)
  • protect from excessive moisture

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


PRINCIPAL DISPLAY PANEL

NDC 41167-4131-4
Allegra
ALLERGY
60 mg/ antihistamine
12 HR
24 TABLETS

NDC 41167-4131-4
Allegra
ALLERGY
60 mg/ antihistamine
12 HR
24 TABLETS

PRINCIPAL DISPLAY PANEL

NDC 41167-4120-3
Allegra
ALLERGY
180 mg/ antihistamine
24 HR
30 TABLETS

NDC 41167-4120-3
Allegra
ALLERGY
180 mg/ antihistamine
24 HR
30 TABLETS

PRINCIPAL DISPLAY PANEL

Allegra
ALLERGY
180 mg/ antihistamine
24 HR
40 TABLETS

Allegra
ALLERGY
180 mg/ antihistamine
24 HR
40 TABLETS

PRINCIPAL DISPLAY PANEL

Allegra
ALLERGY
180 mg/ antihistamine
24 HR
90 TABLETS

Allegra
ALLERGY
180 mg/ antihistamine
24 HR
90 TABLETS

ALLEGRA ALLERGY
fexofenadine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)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)
HYPROMELLOSES (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE (UNII: FZ989GH94E)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
STARCH, CORN (UNII: O8232NY3SJ)
BROWN IRON OXIDE (UNII: 1N032N7MFO)
Product Characteristics
Colororange (peach) Scoreno score
ShapeOVALSize12mm
FlavorImprint Code06;E
Contains
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41167-4131-21 in 1 CARTON03/03/2011
112 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:41167-4131-42 in 1 CARTON03/03/2011
212 in 1 BLISTER PACK; Type 0: Not a Combination Product
3NDC:41167-4131-63 in 1 CARTON03/02/2019
312 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02087203/03/2011
ALLEGRA ALLERGY
fexofenadine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-4120
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)
MAGNESIUM STEARATE (UNII: 70097M6I30)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE (UNII: FZ989GH94E)
STARCH, CORN (UNII: O8232NY3SJ)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
BROWN IRON OXIDE (UNII: 1N032N7MFO)
Product Characteristics
Colororange (peach) Scoreno score
ShapeOVALSize17mm
FlavorImprint Code018;E
Contains
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41167-4120-11 in 1 CARTON03/03/2011
12 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:41167-4120-01 in 1 CARTON03/03/2011
25 in 1 BLISTER PACK; Type 0: Not a Combination Product
3NDC:41167-4120-23 in 1 CARTON03/03/2011
35 in 1 BLISTER PACK; Type 0: Not a Combination Product
4NDC:41167-4120-31 in 1 CARTON03/03/2011
430 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
5NDC:41167-4120-41 in 1 CARTON03/03/2011
545 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
6NDC:41167-4120-52 in 1 CARTON03/03/201107/01/2022
645 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
7NDC:41167-4120-61 in 1 CARTON03/03/2011
770 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02087203/03/2011
ALLEGRA ALLERGY
fexofenadine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-4121
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)
MAGNESIUM STEARATE (UNII: 70097M6I30)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE (UNII: FZ989GH94E)
STARCH, CORN (UNII: O8232NY3SJ)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
BROWN IRON OXIDE (UNII: 1N032N7MFO)
Product Characteristics
Colororange (peach) Scoreno score
ShapeOVALSize17mm
FlavorImprint Code018;E
Contains
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41167-4121-22 in 1 POUCH03/03/201102/18/2020
11 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:41167-4121-32 in 1 PACKAGE03/03/201111/03/2018
21 in 1 BLISTER PACK; Type 0: Not a Combination Product
3NDC:41167-4121-61 in 1 CARTON03/03/201104/04/2017
337 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4NDC:41167-4121-71 in 1 CARTON03/03/201103/03/2017
454 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
5NDC:41167-4121-41 in 1 CARTON03/03/2011
540 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
6NDC:41167-4121-52 in 1 CARTON03/03/201102/01/2018
630 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
7NDC:41167-4121-01 in 1 PACKAGE03/03/201102/18/2020
71 in 1 BLISTER PACK; Type 0: Not a Combination Product
8NDC:41167-4121-11 in 1 CARTON06/01/2021
860 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02087203/03/2011
ALLEGRA ALLERGY
fexofenadine hydrochloride tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-4124
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)
MAGNESIUM STEARATE (UNII: 70097M6I30)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE (UNII: FZ989GH94E)
STARCH, CORN (UNII: O8232NY3SJ)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
BROWN IRON OXIDE (UNII: 1N032N7MFO)
Product Characteristics
ColororangeScoreno score
ShapeOVALSize17mm
FlavorImprint Code018;E
Contains
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41167-4124-71 in 1 CARTON02/01/202104/30/2023
184 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:41167-4124-01 in 1 CARTON12/01/2020
290 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:41167-4124-32 in 1 PACKAGE10/01/2020
3NDC:41167-4124-555 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:41167-4124-81 in 1 CARTON05/01/2022
4100 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02087210/01/2020
Labeler - Chattem, Inc. (003336013)

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