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Fexofenadine

Published: July 26, 2026Updated: August 27, 2026

Fexofenadine is a second-generation antihistamine used to treat seasonal allergic rhinitis (hay fever) and chronic idiopathic urticaria (hives). It works by blocking histamine H1 receptors, reducing allergy symptoms like sneezing, runny nose, and itchy eyes without causing significant drowsiness. This medication is available by prescription and over-the-counter in various forms including tablets, capsules, and oral suspension.

Quick summary

Fexofenadine is a non-drowsy antihistamine that treats seasonal allergies and chronic hives by blocking histamine receptors.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 27, 2026Editorial policy

Key facts at a glance

ATC
R06AX26
RxNorm
87636
Generic
Fexofenadine
Class
atc-r06
Brands
Wal-Fex, Wal-Fex D, Allegra-D, Allegra
Availability
otc
Pregnancy
C
Lactation
caution
Half-life (h)
14.4
Onset (min)
60
Duration (h)
24
Routes
oral
Forms
tablet, orally disintegrating tablet, oral suspension, capsule
Regions
United States, Canada, United Kingdom, European Union, Australia, Japan, India
Monitoring
renal function

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Dosage and administration

adult (standard)tablet
Usual dose
180mg once daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (standard)tablet
Usual dose
30mg twice daily
Maximum
consult physician
Frequency
every 12 hours
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
180mg once daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose of 2000mg or more may cause serious toxicity in adults
Chronic overdose: Prolonged use exceeding recommended daily dose may lead to cumulative CNS depression and anticholinergic effects
Immediate actions
Administer activated charcoal if within 1-2 hours of ingestion, gastric lavage for large recent ingestions, supportive care including airway management
Antidote
No specific antidote exists - treatment is supportive and symptomatic(N/A - supportive care is the mainstay of treatment)
Poison Control: 1-800-222-1222

Special Populations

9 groups
⚠

pregnancy

first trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks; fexofenadine should only be used if clearly needed

Monitor

regular prenatal monitoring

Use with caution and monitor for adverse effects.

⚠

pregnancy

third trimester
caution
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use near term unless benefits outweigh risks

Monitor

fetal monitoring

Use with caution and monitor for adverse effects.

⚠

lactation

breastfeeding
caution
FDA Category
C
Dose Adjustment

use with caution

Key Recommendations

fexofenadine passes into breast milk in small amounts; use only if benefits outweigh risks to infant

Monitor

monitor infant for drowsiness, irritability, or feeding changes

Use with caution and monitor for adverse effects.

⚠

pediatric_age

under 6 years
caution
FDA Category
C
Dose Adjustment

weight-based dosing required

Key Recommendations

use only pediatric formulations; do not exceed recommended dose for age and weight

Monitor

monitor for sedation, dry mouth, urinary retention

Use with caution and monitor for adverse effects.

✓

pediatric_age

6 to 12 years
safe
FDA Category
C
Dose Adjustment

age/weight-based dosing

Key Recommendations

approved for use in children 6 years and older; follow pediatric dosing guidelines

Monitor

standard monitoring for adverse effects

✓

geriatric

over 65 years
safe
FDA Category
C
Dose Adjustment

no specific adjustment required

Key Recommendations

generally well tolerated; use standard adult dosing; consider renal function

Monitor

monitor renal function periodically

✓

renal_impairment

mild to moderate
safe
FDA Category
C
Dose Adjustment

no dose adjustment needed for mild to moderate impairment

Key Recommendations

no dose adjustment required for creatinine clearance above 30 mL/min

Monitor

standard monitoring

⚠

renal_impairment

severe
caution
FDA Category
C
Dose Adjustment

reduce dose to 180mg once daily

Key Recommendations

use reduced dose in severe renal impairment (CrCl less than 30 mL/min)

Monitor

monitor renal function regularly

Use with caution and monitor for adverse effects.

✓

hepatic_impairment

mild to moderate
safe
FDA Category
C
Dose Adjustment

no dose adjustment required

Key Recommendations

no dose adjustment needed for mild to moderate hepatic impairment

Monitor

standard monitoring

Statistics and clinical data

prescribingFDA
2023

FDA Approval Year

Value:1996

FDA approval year for fexofenadine

drug_classWHO
2023

Drug class

Value:Second-generation H1 antihistamine

ATC classification for fexofenadine

usageFDA
2023

Common uses

Value:Treatment of allergic rhinitis and chronic idiopathic urticaria

Therapeutic indications

mechanismFDA
2023

Mechanism of action

Value:Selective peripheral H1 receptor antagonist

Pharmacological mechanism

Fexofenadine is FDA-approved for treatment of seasonal allergic rhinitis (hay fever) in adults and children 2 years and older, as well as chronic idiopathic urticaria (chronic hives) in adults and children 6 months and older. It effectively reduces symptoms including sneezing, rhinorrhea, itchy nose/throat/eyes, and watery eyes associated with allergic reactions.

Fexofenadine is a selective peripheral H1 receptor antagonist. It works by blocking histamine from binding to H1 receptors in various tissues, thereby preventing the inflammatory cascade that causes allergic symptoms. As a second-generation antihistamine, it has reduced ability to cross the blood-brain barrier, which minimizes sedative effects compared to first-generation antihistamines.

Fexofenadine should be avoided in patients with known hypersensitivity to the drug. It may interact with antacids containing aluminum or magnesium, fruit juices, and certain other medications. The medication is generally well-tolerated with common side effects including headache, back pain, and minor gastrointestinal symptoms. Patients with renal impairment may require dose adjustment. Safety during pregnancy should be discussed with a healthcare provider.

Contraindications

Conditions and patient states where this medication should be avoided or used with caution.

Do not use (1)

ABSOLUTEhypersensitivity

Known allergy to this medication or its components

Use caution (1)

RELATIVEpregnancy

Consult healthcare provider for benefits vs risks assessment

Official drug label

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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 27, 2026. · Read our editorial policy