Allegra Allergy: Package Insert / Prescribing Info

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

Medically reviewed by Drugs.com. Last updated on Nov 20, 2024.

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 over	take one 60 mg tablet with water every 12 hours; do not take more than 2 tablets 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

Allegra Allergy Dosage and Administration

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

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

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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

PRINCIPAL DISPLAY PANEL

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

PRINCIPAL DISPLAY PANEL

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

PRINCIPAL DISPLAY PANEL
Allegra
ALLERGY
180 mg/ antihistamine
24 HR
40 TABLETS

PRINCIPAL DISPLAY PANEL

Allegra
ALLERGY
180 mg/ antihistamine
24 HR
90 TABLETS

ALLEGRA ALLERGY
fexofenadine hydrochloride tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:41167-4131
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V)	FEXOFENADINE HYDROCHLORIDE	60 mg

Ingredient Name	Strength
Inactive Ingredients
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
Color	orange (peach)	Score	no score
Shape	OVAL	Size	12mm
Flavor		Imprint Code	06;E
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:41167-4131-2	1 in 1 CARTON	03/03/2011
1		12 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC:41167-4131-4	2 in 1 CARTON	03/03/2011
2		12 in 1 BLISTER PACK; Type 0: Not a Combination Product
3	NDC:41167-4131-6	3 in 1 CARTON	03/02/2019
3		12 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
NDA	NDA020872	03/03/2011

ALLEGRA ALLERGY
fexofenadine hydrochloride tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:41167-4120
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V)	FEXOFENADINE HYDROCHLORIDE	180 mg

Ingredient Name	Strength
Inactive Ingredients
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
Color	orange (peach)	Score	no score
Shape	OVAL	Size	17mm
Flavor		Imprint Code	018;E
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:41167-4120-1	1 in 1 CARTON	03/03/2011	10/01/2019
1		2 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC:41167-4120-0	1 in 1 CARTON	03/03/2011
2		5 in 1 BLISTER PACK; Type 0: Not a Combination Product
3	NDC:41167-4120-2	3 in 1 CARTON	03/03/2011
3		5 in 1 BLISTER PACK; Type 0: Not a Combination Product
4	NDC:41167-4120-3	1 in 1 CARTON	03/03/2011
4		30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
5	NDC:41167-4120-4	1 in 1 CARTON	03/03/2011
5		45 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
6	NDC:41167-4120-5	2 in 1 CARTON	03/03/2011	07/01/2022
6		45 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
7	NDC:41167-4120-6	1 in 1 CARTON	03/03/2011
7		70 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
NDA	NDA020872	03/03/2011

ALLEGRA ALLERGY
fexofenadine hydrochloride tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:41167-4121
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V)	FEXOFENADINE HYDROCHLORIDE	180 mg

Ingredient Name	Strength
Inactive Ingredients
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
Color	orange (peach)	Score	no score
Shape	OVAL	Size	17mm
Flavor		Imprint Code	018;E
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:41167-4121-2	2 in 1 POUCH	03/03/2011	02/18/2020
1		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC:41167-4121-3	2 in 1 PACKAGE	03/03/2011	11/03/2018
2		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
3	NDC:41167-4121-6	1 in 1 CARTON	03/03/2011	04/04/2017
3		37 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4	NDC:41167-4121-7	1 in 1 CARTON	03/03/2011	03/03/2017
4		54 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
5	NDC:41167-4121-4	1 in 1 CARTON	03/03/2011
5		40 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
6	NDC:41167-4121-5	2 in 1 CARTON	03/03/2011	02/01/2018
6		30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
7	NDC:41167-4121-0	1 in 1 PACKAGE	03/03/2011	02/18/2020
7		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
8	NDC:41167-4121-1	1 in 1 CARTON	06/01/2021
8		60 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
NDA	NDA020872	03/03/2011

ALLEGRA ALLERGY
fexofenadine hydrochloride tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:41167-4124
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V)	FEXOFENADINE HYDROCHLORIDE	180 mg

Ingredient Name	Strength
Inactive Ingredients
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
Color	orange	Score	no score
Shape	OVAL	Size	17mm
Flavor		Imprint Code	018;E
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:41167-4124-7	1 in 1 CARTON	02/01/2021	04/30/2023
1		84 in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC:41167-4124-0	1 in 1 CARTON	12/01/2020
2		90 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC:41167-4124-3	2 in 1 PACKAGE	10/01/2020
3	NDC:41167-4124-5	55 in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC:41167-4124-8	1 in 1 CARTON	05/01/2022
4		100 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
NDA	NDA020872	10/01/2020

Labeler - Chattem, Inc. (003336013)

Frequently asked questions

What are the most common skin conditions? (with photos)

More about Allegra Allergy (fexofenadine)

Patient resources

Allegra 12 Hour Allergy drug information

Professional resources

Other formulations

Allegra

Related treatment guides

Medical Disclaimer

Drug Status

Availability Over the counter OTC

Pregnancy & Lactation Risk data available

CSA Schedule* Not a controlled drug N/A

Approval History Drug history at FDA

User Reviews & Ratings

4.7 / 10

12 Reviews

Images

Pill E 018 is Allegra Allergy 24 Hour 180 mg — Allegra Allergy 24 Hour 180 mg (E 018)

Allegra Allergy: Package Insert / Prescribing Info

On This Page

Active ingredient

Purpose

Indications and Usage for Allegra Allergy

Warnings

Do not use

Ask a doctor before use if you have

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding,

Keep out of reach of children.

Allegra Allergy Dosage and Administration

Allegra Allergy Dosage and Administration

Other information

Related/similar drugs

Inactive ingredients

Questions or comments?

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

Frequently asked questions

More about Allegra Allergy (fexofenadine)

Patient resources

Professional resources

Other formulations

Related treatment guides