Active ingredient (in each tablet)

Fexofenadine HCl USP, 180 mg

Purpose

Antihistamine

Uses

Allergy

temporarily relieves these symptoms due to hay fever or otherupper 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 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

180 mg

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.
Store between 20 and 25°C (68 and 77°F)
Protect from excessive moisture
This product meets the requirements of USP Dissolution Test 2

Inactive ingredients

colloidal silicon dioxide, corn starch, croscarmellose sodium, FD&C Red no. 40, hypromellose, iron oxide black, magnesium stearate, mannitol, polyethylene glycol, powder cellulose, and titantium dioxide

Questions?

call 1-888-375-3784

Package Label - 30 Count Carton

carton

Package Label - 30 Count Label

bottle

ALLERGY RELIEF
fexofenadine hydrochloride tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11822-3698(NDC:55111-784)
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)
magnesium stearate (UNII: 70097M6I30)
mannitol (UNII: 3OWL53L36A)
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
FD&C RED NO. 40 (UNII: WZB9127XOA)
HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
polyethylene glycol 400 (UNII: B697894SGQ)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
STARCH, CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	PINK	Score	no score
Shape	OVAL	Size	7mm
Flavor		Imprint Code	194;R
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:11822-3698-1	1 in 1 CARTON	01/03/2011
1		30 in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC:11822-3698-0	3 in 1 CARTON	01/03/2011
2		5 in 1 BLISTER PACK; Type 0: Not a Combination Product
3	NDC:11822-3698-2	1 in 1 CARTON	01/03/2011
3		45 in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC:11822-3698-3	1 in 1 CARTON	01/03/2011
4		90 in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC:11822-3698-4	150 in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2021
6	NDC:11822-3698-5	1 in 1 CARTON	07/23/2023
6		70 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA076502	01/03/2011

Labeler - Rite Aid Corporation (014578892)

Fexofenadine HCl Tablets USP