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Over-the-counter medicine · no prescription needed

Fexofenadine and pseudoephedrine

Purpose on the label: Antihistamine Nasal decongestant

Cough, cold and flu

Official FDA data, not advice

The label text is quoted exactly as the company filed it with the U.S. Food and Drug Administration (FDA), with a link to the official copy. The list of brands comes from the FDA NDC Directory.

This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.

If someone may have taken too much, call Poison Help: 1‑800‑222‑1222. In an emergency, call 911.

Quick answers

What is Fexofenadine and pseudoephedrine used for?
The Drug Facts label of Equate Allergy Relief D (Walmart Inc.) lists these 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; temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies; reduces swelling of nasal passages; temporarily relieves sinus congestion and pressure; temporarily restores freer breathing through the nose.
Do I need a prescription for Fexofenadine and pseudoephedrine?
No. The products on this page are sold without a prescription (over the counter).
Is a store brand the same as the name brand?
Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
Has Fexofenadine and pseudoephedrine been recalled?
FDA enforcement reports list 5 recalls of products on this page; the newest started January 4, 2022. A recall usually concerns specific products or lots, not every brand.

Drug Facts label

Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.

Equate Allergy Relief D · Walmart Inc.

Fexofenadine hydrochloride 60 mg · Pseudoephedrine hydrochloride 120 mg, tablet, film coated, extended release (oral)

Active ingredient (in each tablet)

Fexofenadine HCl 60 mg Pseudoephedrine HCl 120 mg

Purpose

Antihistamine Nasal decongestant

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
  • temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies
  • reduces swelling of nasal passages
  • temporarily relieves sinus congestion and pressure
  • temporarily restores freer breathing through the nose

Warnings

Do not use

  • if you have ever had an allergic reaction to this product or any of its ingredients
  • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
  • if you have difficulty swallowing

Ask a doctor before use if

you have

  • heart disease
  • thyroid disease
  • glaucoma
  • high blood pressure
  • diabetes
  • trouble urinating due to an enlarged prostate gland
  • 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)
  • the tablet coating may be seen in the stool (this is normal). Continue to take as directed (see Directions).

Stop use and ask a doctor if

  • an allergic reaction to this product occurs. Seek medical help right away.
  • symptoms do not improve within 7 days or are accompanied by a fever
  • you get nervous, dizzy, or sleepless

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

do not divide, crush, chew or dissolve the tablet; swallow tablet whole

  • adults and children 12 years of age and over
  • take 1 tablet with a glass of water every 12 hours on an empty stomach; do not take more than 2 tablets 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

  • each tablet contains: calcium 21 mg
  • 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)
  • meets USP Dissolution Test 2

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, D&C yellow #10 aluminum lake, dibasic calcium phosphate dihydrate, FD&C blue #2 aluminum lake, FD&C yellow #6 aluminum lake, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, pregelatinized starch

Questions?

1-888-287-1915

— FDA label of Equate Allergy Relief D, Walmart Inc., effective August 3, 2026. See the official label on DailyMed →

Fexofenadine HCl and Pseudoephedrine HCI · Dr. Reddy's Laboratories Limited

Fexofenadine hydrochloride 60 mg · Pseudoephedrine hydrochloride 120 mg, tablet, extended release (oral)

Active ingredient (s)

Fexofenadine HCl USP, 60 mg Pseudoephedrine HCl USP,120 mg

Purpose

Antihistamine Nasal decongestant

Uses

(s) 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 temporarily relives nasal congestion due tothe common cold, hay fever or other upper respiratory allergies reduces swelling of nasal passages temporarily relieves sinus congestion and pressure temporarily restores freer breathing through the nose

Warnings

Do not use

if you have ever had an allergic reaction to this product or any of its ingredients if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. if you have difficulty swallowing

Ask a doctor before use if

you have heart disease thyroid disease glaucoma high blood pressure diabetes trouble urinating due to an enlarged prostate gland 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) the tablet coating may be seen in the stool (this is normal). Continue to takeas directed (see Directions). Stop use and ask doctor if an allergic reaction to this product occurs. Seek medical help right away. symptoms do not improve within 7 days or are accompanied by a fever you get nervous, dizzy, or sleepless

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

do not divide, crush, chew or dissolve the tablet; swallow tablet whole

adults and children 12 years of age and over take 1 tablet with a glass of water every 12 hours on an empty stomach; do not take more than 2 tablets in 24 hours
children under 12 years of agedo not use
adults 65 years of age and olderask a doctor
consumers with kidney diseaseask a doctor

Inactive ingredients

corn starch, croscarmellose sodium, colloidal silicon dioxide, ferric oxide, hypromellose, kollidon SR, magnesium stearate, mannitol, powder cellulose and triethyl citrate.

Questions?

call 1-888-375-3784 Manufactured by: Dr. Reddy’s Laboratories Limited Bachupally - 500 090 INDIA

— FDA label of Fexofenadine HCl and Pseudoephedrine HCI, Dr. Reddy's Laboratories Limited, effective December 19, 2024. See the official label on DailyMed →

Allegra-D Allergy and Congestion · Chattem, Inc.

Fexofenadine hydrochloride 180 mg · Pseudoephedrine hydrochloride 240 mg, tablet, film coated, extended release (oral)

Active ingredient (in each extended-release tablet)

Fexofenadine HCl 180 mg Active ingredients (in each extended-release tablet) Pseudoephedrine HCl 240 mg

Purpose

Antihistamine Purpose Nasal decongestant

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 temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies reduces swelling of nasal passages temporarily relieves sinus congestion and pressure temporarily restores freer breathing through the nose

Warnings

Do not use

if you have ever had an allergic reaction to this product or any of its ingredients if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. If you have difficulty swallowing

Ask a doctor before use if

you have heart disease thyroid disease glaucoma high blood pressure diabetes trouble urinating due to an enlarged prostate gland 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 ) the tablet coating may be seen in the stool (this is normal). Continue to take as directed (see Directions ).

Stop use and ask a doctor if

an allergic reaction to this product occurs. Seek medical help right away. symptoms do not improve within 7 days or are accompanied by a fever you get nervous, dizzy, or sleepless

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

do not divide, crush, chew or dissolve the tablet; swallow tablet whole

adults and children 12 years of age and overtake 1 tablet with a glass of water every 24 hours on an empty stomach; do not take more than 1 tablet in 24 hours
children under 12 years of agedo not use
adults 65 years of age and olderask a doctor
consumers with kidney diseaseask a doctor

Inactive ingredients

acetone, black iron oxide, cellulose acetate, colloidal silicon dioxide, copovidone, croscarmellose sodium, FD&C blue #1 aluminum lake, glycerol triacetate, hypromellose, isopropyl alcohol, magnesium stearate, microcrystalline cellulose, polyethylene glycol, propylene glycol, povidone, sodium chloride, talc, titanium dioxide, water

Questions?

call toll-free 1-800-633-1610 or www.allegra.com

— FDA label of Allegra-D Allergy and Congestion, Chattem, Inc., effective January 12, 2026. See the official label on DailyMed →

Fexofenadine HCl and Pseudoephedrine HCI · Dr.Reddy's Laboratories Limited

Fexofenadine hydrochloride 180 mg · Pseudoephedrine hydrochloride 240 mg, tablet, extended release (oral)

Active ingredient (s)

Fexofenadine HCl USP, 180 mg Pseudoephedrine HCl USP, 240 mg

Purpose

Antihistamine Nasal decongestant

Uses

(s) 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 temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies reduces swelling of nasal passages temporarily relieves sinus congestion and pressure temporarily restores freer breathing through the nose

Warnings

Do not use

if you have ever had an allergic reaction to this product or any of its ingredients if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. if you have difficulty swallowing

Ask a doctor before use if

you have heart disease thyroid disease glaucoma high blood pressure diabetes trouble urinating due to an enlarged prostate gland 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) the tablet coating may be seen in the stool (this is normal). Continue to take as directed (see Directions). Stop use and ask doctor if an allergic reaction to this product occurs. Seek medical help right away. symptoms do not improve within 7 days or are accompanied by a fever you get nervous, dizzy, or sleepless

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

do not divide, crush, chew or dissolve the tablet; swallow tablet whole

adults and children 12 years of age and over take 1 tablet with a glass of water every 24 hours on an empty stomach; do not take more than 1 tablet in 24 hours
children under 12 years of agedo not use
adults 65 years of age and olderask a doctor
consumers with kidney diseaseask a doctor

Inactive ingredients

acetyltributyl citrate, colloidal silicon dioxide, copovidone, croscarmellose sodium, ethylcellulose, hydrogenated vegetable oil, hypromellose, microcrystalline cellulose, polyethylene glycol, sodium stearyl fumarate, talc and titanium dioxide.

Questions?

Call 1-888-375-3784 Manufactured by: Dr. Reddy’s Laboratories Limited Bachupally - 500 090 INDIA.

— FDA label of Fexofenadine HCl and Pseudoephedrine HCI, Dr.Reddy's Laboratories Limited, effective December 5, 2018. See the official label on DailyMed →

This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.

Same medicine, other brands

Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.

Fexofenadine hydrochloride 60 mg · Pseudoephedrine hydrochloride 120 mg · tablet, film coated, extended release (oral) · 18 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Allegra-D A-S Medication Solutions DailyMed
Allegra-D Allergy and Congestion Chattem, Inc. DailyMed
Equate Allergy Relief D Walmart Inc. DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride AmeriSource Bergen DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Aurohealth LLC DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Cardinal Health DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride CVS Pharmacy DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride CVS Pharmacy, Inc. DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride H E B DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Kroger Company DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Ohm Laboratories Inc. DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Rugby Laboratories DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Sun Pharmaceutical Industries, Inc. DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Walgreen Co. DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Walgreens DailyMed
Foster and Thrive Allergy and Congestion D Strategic Sourcing Services LLC DailyMed
Leader 12hr Allergy and Congestion Relief Cardinal Health 110, LLC. dba Leader DailyMed
Rugby Allergy Relief D Rugby Laboratories DailyMed
Fexofenadine hydrochloride 60 mg · Pseudoephedrine hydrochloride 120 mg · tablet, extended release (oral) · 16 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Allergy and Congestion Rite Aid Corporation DailyMed
Fexofenadine HCl and Pseudoephedrine HCI CVS Pharmacy DailyMed
Fexofenadine HCl and Pseudoephedrine HCI Dr. Reddy's Laboratories Inc. DailyMed
Fexofenadine HCl and Pseudoephedrine HCI Dr. Reddy's Laboratories Limited DailyMed
Fexofenadine HCl and Pseudoephedrine HCI Heb DailyMed
Fexofenadine HCl and Pseudoephedrine HCI The Kroger Co. DailyMed
Fexofenadine HCl and Pseudoephedrine HCI Walgreens Company DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride CVS Health Corp DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride CVS Pharmacy DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Kroger Company DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Publix Super Markets, Inc DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Rite Aid Corporation DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Strategic Sourcing Services, LLC DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Wal-mart Stores, Inc. DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Walgreens Company DailyMed
Fexofenadine hydrochloride 180 mg · Pseudoephedrine hydrochloride 240 mg · tablet, film coated, extended release (oral) · 3 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Allegra-D Allergy and Congestion Chattem, Inc. DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Aurohealth LLC DailyMed
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Walgreen Co. DailyMed
Fexofenadine hydrochloride 180 mg · Pseudoephedrine hydrochloride 240 mg · tablet, extended release (oral) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Fexofenadine HCl and Pseudoephedrine HCI Dr.Reddy's Laboratories Limited DailyMed

What pharmacies pay (NADAC)

The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.

This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.

NADAC per unit for Fexofenadine and pseudoephedrine, by strength and form
Strength and formGeneric or brandPharmacies pay
fexofenadine hydrochloride 60 mg · pseudoephedrine hydrochloride 120 mg
tablet, extended release
Generic $0.4769 per tablet
fexofenadine hydrochloride 60 mg · pseudoephedrine hydrochloride 120 mg
tablet, film coated, extended release
Generic $0.4769 per tablet

NADAC list of November 4, 2026; these prices took effect on October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.

Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →

Companies that sell this medicine

The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.

Recalls

From FDA enforcement reports, matched by the product’s NDC code or label. A recall usually covers specific products or lots: check the name and lot number on your package.

  1. January 4, 2022 · Class III · Terminated · D-0378-2022

    Failed Dissolution Specifications

    Wal-Fex D, Fexofenadine HCl 60mg/Antihistamine & Pseudoephedrine HCl 120mg/Nasal Decongestant, Extended Release Tablets USP, a) 20 Extended Release Tablets per box, NDC 0363-1606-20, b) 30 Extended Release Tablets per bo — Dr. Reddy's Laboratories, Inc.

  2. January 4, 2022 · Class III · Terminated · D-0381-2022

    Failed Dissolution Specifications

    Kroger, Allergy Relief-D, Fexofenadine HCl 60mg/Antihistamine Pseudoephedrine HCl 120mg/Nasal Decongestant, Extended-Release Tablets USP, 20 tablets per box, NDC 30142-611-14, Distributed by the Kroger Co., Cincinnati, O — Dr. Reddy's Laboratories, Inc.

  3. November 12, 2021 · Class III · Terminated · D-0267-2022

    Failed dissolution specifications

    Allergy & Congestion Fexofenadine HCl 60 mg & Pseudoephedrine HCl 120 mg Extended-Release Tablets, USP, 20 Extended-Release Tablets, Distributed by: Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-7388-5. — Dr. Reddy's Laboratories, Inc.

  4. November 12, 2021 · Class III · Terminated · D-0275-2022

    Failed dissolution specifications

    Fexofenadine HCl, 60 mg & Pseudoephedrine HCl 120 mg, Extended Release Tablets USP, Allergy and Congestion, 30 Tablets, Distributed by: Dr. Reddy's Laboratories, Inc., Princeton, NJ, 08640, Made in India NDC Walmart Inc. — Dr. Reddy's Laboratories, Inc.

  5. November 12, 2021 · Class III · Terminated · D-0269-2022

    Failed dissolution specifications

    Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended Release Tablets USP Allergy & Congestion, 20 Tablets, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ 08540, NDC 43598-823-14. — Dr. Reddy's Laboratories, Inc.

Sources

  1. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  4. FDA rule for the Drug Facts label (21 CFR 201.66)

Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.

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