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Fexofenadine HCl

Dosage form
TABLET
Labeler
Rite Aid
Label updated
2025-12-19
Retrieved
2026-09-07
Active ingredients
FEXOFENADINE HYDROCHLORIDE
View original label and images on DailyMed ↗
Active ingredient (in each tablet)

Fexofenadine HCl USP, 60 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

W​arnings

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.

Directions

adults and children take one 60 mg tablet with water every 12 hours; do not take more than 2 tablets in 24 hours

12 years of age and over


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

■ safety sealed: do not use if carton is opened or if individual blister units are torn or opened ■ store between
20° and 25°C (68° and 77°F) ■ protect from excessive moisture

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?

contact 1-877-770-3183 Mon-Fri 8:00 AM EST to 5:00 PM PST

PDP

[Image in the official label — see DailyMed source]

DailyMed Set ID: 1ddb1716-9c5b-6348-e063-6394a90acbf1 · Version 3
NDC: 11822-7652