Allergy Relief by Big Lots DRUG FACTS

Allergy Relief by

Drug Labeling and Warnings

Allergy Relief by is a Otc medication manufactured, distributed, or labeled by Big Lots. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALLERGY RELIEF- fexofenadine hcl tablet, coated 
Big Lots

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DRUG FACTS

Active ingredient (in each tablet)

Fexofenadine HCl USP 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 (1-800-222-1222) right away

Directions

• adults and children 12 years of age and over:

  take one 18 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

• store between 20-25ºC (68-77ºF)
• protect from excessive moisture

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, hypromellose, iron oxide black, iron oxide red, iron oxide yellow, lactose monohydrate, pregelatinized starch (maize), polyethylene glycol, magnesium stearate, microcrystalline cellulose, titanium dioxide

Questions or comments?

Call 1-877-753-3935 Monday-Friday9AM-5PM EST

Principal Display Panel

*Compare to the active ingredient in Allegra® Allergy 24 Hour

NON-DROWSY

Allergy Relief

Fexofenadine HCl Tablets USP, 180 mg

Antihistamine Indoor & Outdoor Allergies

24 Hour Relief of: Runny Nose; Sneezing; Itchy, Watery Eyes; Itchy Nose or Throat

CAPLETS**

(**Capsule-Shaped Tablets)

*This product is not manufactured or distributed by Chattem Inc., distributor of Allegra® Allergy 24 Hour.

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION

Distributed by:

Big Lots Stores, Inc.

P.O. Box 28523

Columbus, OH 43228-0523

  

Product Label

SOUND BODY Non-Drowsy Allergy Relief

ALLERGY RELIEF 
fexofenadine hcl tablet, coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50594-801
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V)	FEXOFENADINE HYDROCHLORIDE	180 mg

Inactive Ingredients
Ingredient Name	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
HYPROMELLOSES (UNII: 3NXW29V3WO)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
MAGNESIUM STEARATE (UNII: 70097M6I30)
STARCH, CORN (UNII: O8232NY3SJ)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)

Product Characteristics
Color	pink	Score	no score
Shape	CAPSULE	Size	17mm
Flavor		Imprint Code	G6
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50594-801-30	1 in 1 BOX	08/20/2021	12/31/2025
1		30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA204507	08/20/2021	12/31/2025

Labeler - Big Lots (017885351)

Revised: 6/2025

Document Id: a12f073b-587e-4fb5-ab4d-e5f890406464

34390-5

Set id: 3a445198-4dd1-4b8a-bf86-3518b00a8b3b

Version: 5

Effective Time: 20250616