Fexofenadine Hcl Tablet
FDA Label NDC 50090-6965

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by A-s Medication Solutions for the product Fexofenadine Hcl (NDC 50090-6965). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient(s) in each tablet, purpose, use(s), do not use, ask a doctor before use if, when using this product, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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

 adults and children 12 years of age and overtake 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

        • Tamper-Evident: Do not use if printed foil seal under cap is missing
• store between 20° and 25°C (68° and 77°F)
• protect from excessive moisture


Inactive Ingredients

Colloidal silicon dioxide, hypromellose, light liquid paraffin, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polysorbate 80, pregelatinized starch, red iron oxide, sodium starch glycolate, talc, titanium dioxide and yellow iron oxide.

Questions?

Call 1-800-206-7821

Manufactured for:
Northstar Rx LLC
Memphis, TN 38141.

Manufactured by:
Hetero Labs Limited,
Unit V, Polepally, Jadcherla,
Mahabubnagar - 509 301, India.

Mfg. Lic. No.: 50/MN/AP/2009/F/R

Issued: 04/2019

* Please review the disclaimer below.