ALLERGY RELIEF- fexofenadine hcl tablet, film coated

ALLERGY RELIEF by

Drug Labeling and Warnings

ALLERGY RELIEF by is a Otc medication manufactured, distributed, or labeled by Bi-Mart, ScieGen Pharmaceuticals, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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
• sneezing
• itchy, watery eyes
• 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 180mg 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° and 25°C (68° and 77°F)
• protect from excessive moisture
• each tablet contains: sodium 8 mg
• this product meets the requirements of USP Dissolution Test 2

Inactive ingredients

anhydrous lactose, colloidal silicon dioxide, corn starch, croscarmellose sodium, hypromellose, lactose monohydrate, polyethylene glycol, pregelatinized starch(maize), red iron oxide, stearic acid, titanium dioxide, yellow iron oxide.

Questions?

Call toll-free  1-844-912-4012

PRINCIPAL DISPLAY PANEL

NDC: 37835-601-09

COMPARE TO THE ACTIVE INGREDIENT IN ALLEGRA ®ALLERGY 24 HOUR TABLETS*

NON-DROWSY

ALLERGY RELIEF

FEXOFENADINE HYDROCHLORIDE 180 mg

24 HOUR ALLERGY

ORIGINAL PRESCRIPTION STRENGTH

RELIEF OF:

SNEEZING

RUNNY NOSE

ITCHY, WATER EYES

ITCHY NOSE OR THROAT

ANTIHISTAMINE

90 Tablets

*This product is not manufactured or distributed by the owner of the registered trademark Allegra ®Allergy 24 Hour Tablets.

Distributed by:

BI-MART

Eugene, OR 97402

PRINCIPAL DISPLAY PANEL

NDC: 37835-601-45

COMPARE TO THE ACTIVE INGREDIENT IN ALLEGRA ®ALLERGY 24 HOUR TABLETS*

NON-DROWSY

ALLERGY RELIEF

FEXOFENADINE HYDROCHLORIDE 180 mg

24 HOUR ALLERGY

ORIGINAL PRESCRIPTION STRENGTH

RELIEF OF:

SNEEZING

RUNNY NOSE

ITCHY, WATER EYES

ITCHY NOSE OR THROAT

ANTIHISTAMINE

45 Tablets

*This product is not manufactured or distributed by the owner of the registered trademark Allegra ®Allergy 24 Hour Tablets.

Distributed by:

BI-MART

Eugene, OR 97402

INGREDIENTS AND APPEARANCE

ALLERGY RELIEF 
fexofenadine hcl tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37835-601
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
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STARCH, CORN (UNII: O8232NY3SJ)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
STEARIC ACID (UNII: 4ELV7Z65AP)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
FERRIC OXIDE RED (UNII: 1K09F3G675)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)

Product Characteristics
Color	pink	Score	no score
Shape	OVAL	Size	18mm
Flavor		Imprint Code	SG202
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37835-601-45	45 in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2025
2	NDC: 37835-601-09	90 in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA204507	09/16/2015

Labeler - Bi-Mart (027630078)

Establishment
Name	Address	ID/FEI	Business Operations
ScieGen Pharmaceuticals, INC.		079391286	manufacture(37835-601)