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FLONASE ALLERGY RELIEF 50 ug/1

fluticasone propionate · SPRAY, METERED · Haleon US Holdings LLC

No Recall HistoryCurrently in Shortage
Plain English

FLONASE ALLERGY RELIEF is a spray, metered containing fluticasone propionate at 50 ug/1, taken nasal. Manufactured by Haleon US Holdings LLC.

Key Facts

Brand Name
FLONASE ALLERGY RELIEF
Generic Name
fluticasone propionate
NDC Code (Product)
0135-0576
Manufacturer
Haleon US Holdings LLC
Strength
50 ug/1
Dosage Form
SPRAY, METERED
Route
NASAL
Marketing Status
Application #
NDA205434
Marketing Start
12/04/2014

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective7,592 reports
headache6,004 reports
fatigue5,964 reports
dyspnoea5,906 reports
nausea5,247 reports
pain4,591 reports
diarrhoea4,455 reports
cough4,137 reports
off label use4,121 reports
dizziness3,921 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • runny nose • sneezing • itchy nose • itchy, watery eyes

Dosage & Administration

Directions • read the Quick Start Guide for how to: o prime the bottle o use the spray o clean the spray nozzle • shake gently before each use • use this product only once a day • do not use more than directed ADULTS AND CHILDREN 12 YEARS OF AGE AND OLDER • Week 1- use 2 sprays in each nostril once daily • Week 2 through 6 months- use 1 or 2 sprays in each nostril once daily, as needed to treat your symptoms • After 6 months of daily use – ask your doctor if you can keep using CHILDREN 4 TO 11 YEARS OF AGE • the growth rate of some children may be slower while using this product. Children should use for the shortest amount of time necessary to achieve symptom relief. Talk to your child’s doctor if your child needs to use the spray for longer than two months a year. • an adult should supervise use • use 1 spray in each nostril once daily CHILDREN UNDER 4 YEARS OF AGE • do not use

Warnings

Warnings Only for use in the nose. Do not spray into your eyes or mouth. Do not use • in children under 4 years of age • to treat asthma • if you have an injury or surgery to your nose that is not fully healed • if you have ever had an allergic reaction to this product or any of the ingredients Ask a doctor before use if you have or had glaucoma or cataracts Ask a doctor or pharmacist before use if you are taking • medicine for HIV infection (such as ritonavir) • a steroid medicine for asthma, allergies or skin rash • ketoconazole pills (medicine for fungal infection) When using this product • the growth rate of some children may be slower • stinging or sneezing may occur for a few seconds right after use • do not share this bottle with anyone else as this may spread germs • remember to tell your doctor about all the medicines you take, including this one Stop use and ask a doctor if • you have, or come into contact with someone who has, chicken pox, measles or tuberculosis • your symptoms do not get better within 7 days of starting use or you get new symptoms such as severe facial pain or thick nasal discharge. You may have something more than allergies, such as an infection. • yo

Frequently Asked Questions

What is FLONASE ALLERGY RELIEF used for?

FLONASE ALLERGY RELIEF contains fluticasone propionate. It is a spray, metered taken nasal. Consult your doctor for specific uses.

Is FLONASE ALLERGY RELIEF a controlled substance?

FLONASE ALLERGY RELIEF is not classified as a controlled substance by the DEA.

What is the generic name for FLONASE ALLERGY RELIEF?

The generic name for FLONASE ALLERGY RELIEF is fluticasone propionate. There are 11 other brand versions of fluticasone propionate.

What is the NDC code for FLONASE ALLERGY RELIEF 50 ug/1?

The NDC (National Drug Code) for FLONASE ALLERGY RELIEF 50 ug/1 is 0135-0576, listed by Haleon US Holdings LLC.