ALLEGRA ALLERGY- fexofenadine hydrochloride tablet, film coated

Allegra Allergy by

Drug Labeling and Warnings

Allegra Allergy by is a Otc medication manufactured, distributed, or labeled by Select Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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:

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

Directions

• 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 the individual blister unit is torn or opened
• 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

SPL UNCLASSIFIED SECTION

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

INGREDIENTS AND APPEARANCE

ALLEGRA ALLERGY 
fexofenadine hydrochloride tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52904-190(NDC:41167-4131)
Route of Administration	ORAL

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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52904-190-03	1 in 1 BLISTER PACK	12/08/2021
1		1 in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NDA	NDA020872	12/08/2021

Labeler - Select Corporation (053805599)