FEXOFENADINE HYDROCHLORIDE- fexofenadine hydrochloride tablet 
CVS Health Corp.

----------

Fexofenadine HCl Tablets USP

Active ingredient (in each tablet)

Fexofenadine HCl USP, 180 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or otherupper 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 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 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, corn starch, croscarmellose sodium, FD&C Red no. 40, hypromellose, iron oxide black, magnesium stearate, mannitol, polyethylene glycol, powder cellulose and titanium dioxide.

Questions?

Call 1-888-375-3784

Carton label

Carton Label: 40 count

CVS Health

Compare to the active ingedient in
Allegra® Allergy 24 Hour Tablets*

Indoor & Outdoor Alllergies

Original Prescription Strength

Allergy Relief

FEXOFENADINE HYDROCHLORIDE
TABLETS USP, 180 MG

24 Hour Relief of:

Non-Drowsy 24 HOUR

Actual Bottle Size on Bottom Panel

Package Contains One Bottle

40 TABLETS 180 mg EACH

Carton

Bottle Label

Bottle Label: 40 count

CVS Health

Compare to the active ingedient in
Allegra® Allergy 24 Hour Tablets*

Indoor & Outdoor Alllergies

Original Prescription Strength

Allergy Relief

FEXOFENADINE HYDROCHLORIDE
TABLETS USP, 180 MG

24 Hour Relief of:

Non-Drowsy 24 HOUR

Actual Bottle Size on Bottom Panel

Package Contains One Bottle

40 TABLETS 180 mg EACH

Bottle

FEXOFENADINE HYDROCHLORIDE 
fexofenadine hydrochloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-052(NDC:55111-784)
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)  
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
ColorPINKScoreno score
ShapeOVALSize7mm
FlavorImprint Code 194;R
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-052-301 in 1 CARTON04/01/2011
130 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:69842-052-901 in 1 CARTON04/01/2011
290 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:69842-052-401 in 1 CARTON05/01/2013
340 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:69842-052-451 in 1 CARTON04/01/2011
445 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:69842-052-602 in 1 CARTON04/01/2011
560 in 1 CARTON; Type 0: Not a Combination Product
6NDC:69842-052-181 in 1 CARTON02/01/2013
6180 in 1 CARTON; Type 0: Not a Combination Product
7NDC:69842-052-021 in 1 CARTON04/01/2015
72 in 1 BLISTER PACK; Type 0: Not a Combination Product
8NDC:69842-052-071 in 1 CARTON04/01/2011
85 in 1 BLISTER PACK; Type 0: Not a Combination Product
9NDC:69842-052-153 in 1 CARTON04/01/2011
95 in 1 BLISTER PACK; Type 0: Not a Combination Product
10NDC:69842-052-293 in 1 CARTON04/01/2011
1015 in 1 BLISTER PACK; Type 0: Not a Combination Product
11NDC:69842-052-701 in 1 CARTON01/11/2019
1170 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07650204/01/2011
Labeler - CVS Health Corp. (062312574)

Revised: 12/2021
Document Id: 704d6528-78b3-f58e-42d6-91175ceb49ea
Set id: 204506d7-7688-fd7e-0aae-142b698848ef
Version: 8
Effective Time: 20211220
 
CVS Health Corp.