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Fexofenadine HCL

Dosage form
TABLET
Labeler
Akron Pharma Inc.
Label updated
2024-08-20
Retrieved
2026-09-07
Active ingredients
FEXOFENADINE HYDROCHLORIDE
View original label and images on DailyMed ↗
ACTIVE INGREDIENT(S), in each tablet

Fexofenadine hydrochloride USP, 180 mg

PURPOSE

Antihistamine

USE(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

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

60 mg

adults and children 12 years of age and over take one 60 mg tablet with water every 12 hours; 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

180 mg

adults and children 12 years of age and over take one 180 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
  • Safety Sealed: do not use if carton is opened or if printed foil inner seal on the bottle is torn or missing.
  • store between 20° and 25°C (68° and 77°F)
  • protect from excessive moisture
INACTIVE INGREDIENTS

anhydrous lactose, colloidal silicon dioxide, corn starch, croscarmellose sodium, lactose monohydrate, pregelatinized starch(maize), stearic acid, opadry pink 03B84893 containing hypromellose, polyethylene glycol, red iron oxide titanium dioxide and yellow iron oxide.

HOW SUPPLIED SECTION

Fexofenadine Hydrochloride Tablets, USP 180 mg 30 CT 

NDC: 71399-8042-3

Fexofenadine Hydrochloride Tablets, USP 180 mg 100 CT

NDC: 71399-8042-1

QUESTIONS OR COMMENTS

Call weekdays 8.30 AM to 4.30 PM EST Please Call 1(877) 225-6999

Manufactured for:
Akron Pharma, Inc.
Fairfield, NJ 07004
Manufactured in U.S.A

포장 표시

[Image in the official label — see DailyMed source]

[Image in the official label — see DailyMed source]

DailyMed Set ID: 08023b99-0634-4ac9-afd6-4f2d2e0d2c8a · Version 4
NDC: 71399-8042