ALLERGY RELIEF- fexofenadine hydrochloride tablet 
HEB

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1192B-HEB-2022-0328

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:

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 (1-800-222-1222).

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

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, hypromellose, iron oxide black, iron oxide red, iron oxide yellow, lactose monohydrate, macrogol, magnesium stearate, microcrystalline cellulose, pregelatinized starch, titanium dioxide

Questions or comments?

1-844-705-4384

PRINCIPAL DISPLAY PANEL

Compare to Allegra® Allergy 24 Hour active ingredient†

HEB®

NDC 37808-392-03

Allergy Relief

Fexofenadine Hydrochloride

Tablets, 180mg/Antihistamine

NON-DROWSY

INDOOR/OUTDOOR ALLERGY RELIEF

24 hour

• Sneezing

• Runny Nose

• Itchy, Watery Eyes

• Itchy Nose or Throat

15 TABLETS

actual size

image description

ALLERGY RELIEF 
fexofenadine hydrochloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-392
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
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
STARCH, CORN (UNII: O8232NY3SJ)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
Colororange ((PEACH)) Scoreno score
ShapeOVAL (Capsule-shaped) Size17mm
FlavorImprint Code G6
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-392-033 in 1 CARTON05/31/2022
15 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:37808-392-171 in 1 CARTON05/31/2022
230 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:37808-392-181 in 1 CARTON05/31/2022
340 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4NDC:37808-392-191 in 1 CARTON05/31/2022
445 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
5NDC:37808-392-2090 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/31/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21107505/31/2022
Labeler - HEB (007924756)

Revised: 5/2022
Document Id: e051ea08-74a0-5897-e053-2a95a90a7efd
Set id: d8b852a1-7315-4047-aed6-cd40c7a39e70
Version: 3
Effective Time: 20220531
 
HEB