Hy-Vee, Inc. Allergy Relief Drug Facts

allergy relief by

Drug Labeling and Warnings

allergy relief by is a Otc medication manufactured, distributed, or labeled by HyVee Inc, L. Perrigo Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALLERGY RELIEF- fexofenadine hcl tablet, film coated 
HyVee Inc

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Hy-Vee, Inc. Allergy Relief 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. (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

  • do not use if blister unit is broken or torn (Use with blister unit configuration only)
  • do not use if printed foil under cap is broken or missing (Use with bottle/carton configuration only)
  • store at 20°-25°C (68°-77°F)
  • protect from excessive moisture
  • this product meets the requirements of USP Dissolution Test 3

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, hypromellose, iron oxide black, iron oxide red, iron oxide yellow, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, titanium dioxide

Questions or comments?

1-800-719-9260

Package/Label Principal Display Panel

Compare to the Active Ingredient of Allegra® Allergy Tablets

Non-Drowsy

Allergy Relief

FEXOFENADINE HYDROCHLORIDE TABLETS, 180 mg/ANTIHISTAMINE

Indoor & Outdoor Allergies

Relief of:

Sneezing

Runny Nose

Itchy, Watery Eyes

Itchy Nose or Throat

ORIGINAL PRESCRIPTION STRENGTH

ACTUAL SIZE

24 HOUR

45 Tablets 180 mg EACH

Allergy Relief Image 1
Allergy Relief Image 2
ALLERGY RELIEF 
fexofenadine hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 42507-692
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)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
POVIDONE (UNII: FZ989GH94E)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorORANGE (peach) Scoreno score
ShapeROUNDSize12mm
FlavorImprint Code 93;7253
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 42507-692-951 in 1 CARTON02/12/201402/19/2019
145 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC: 42507-692-761 in 1 CARTON02/12/201412/19/2016
2120 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC: 42507-692-391 in 1 CARTON02/12/201401/29/2019
330 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC: 42507-692-135 in 1 CARTON02/12/201410/29/2018
41 in 1 BLISTER PACK; Type 0: Not a Combination Product
5NDC: 42507-692-2215 in 1 CARTON02/12/201403/05/2019
51 in 1 BLISTER PACK; Type 0: Not a Combination Product
6NDC: 42507-692-011 in 1 CARTON02/12/201401/13/2019
670 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07644702/12/201403/05/2019
Labeler - HyVee Inc (006925671)

Revised: 11/2019
Document Id: 61d08114-e360-43a4-96a8-7bc331dffcd6
Set id: 879bbd56-2cad-4eb1-b3fa-69af277f7f58
Version: 4
Effective Time: 20191115
 
HyVee Inc