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Flonase Allergy Relief : Package Insert / Prescribing Info

Package insert / product label
Generic name: fluticasone propionate
Dosage form: nasal spray, metered
Drug class: Nasal steroids

Medically reviewed by Drugs.com. Last updated on Jan 8, 2025.

Active Ingredient (in each spray)

Fluticasone propionate (glucocorticoid)* 50 mcg
*read the Question & Answer Leaflet

Purpose

Allergy symptom reliever

Indications and Usage for Flonase Allergy Relief

Temporarily relieves these symptoms of hay fever or other upper respiratory allergies:

nasal congestion
itchy nose
runny nose
itchy, watery eyes
sneezing

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.
you get a constant whistling sound from your nose. This may be a sign of damage inside your nose.
you get an allergic reaction to this product. Seek medical help right away.
you get new changes to your vision that develop after starting this product
you have severe or frequent nosebleeds

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.

Flonase Allergy Relief Dosage and Administration

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

Storage and Handling

you may start to feel relief the first day and full effect after several days of regular, once-a-day use
store between 4° and 30°C (39° and 86°F)
keep this label and enclosed materials. They contain important additional information.

Inactive ingredients

benzalkonium chloride, dextrose, microcrystalline cellulose, phenylethylalcohol, polysorbate 80, purified water, sodium carboxymethylcellulose

Questions or comments?

call toll-free 1-844-FLONASE (1-844-356-6273)

Generic Section

What problems can FLONASE Allergy Relief help with?

FLONASE Allergy Relief helps relieve a broad range of uncomfortable symptoms like congestion and itchy eyes.

Nasal symptoms

Eye symptoms

These symptoms can be triggered by allergens like pollen, mold, dust or pet dander.

Outdoor allergens

Animal allergens

Indoor allergens

IMPORTANT – Peel here for complete Drug Facts label. Children 4-11: do not use for more than 2 months a year.

Be sure to read the Quick Start Guide and Question & Answer Leaflet inside package

TAMPER-EVIDENTfeatures for your protection. The product is packaged in a sealed container. Under the cap and nozzle, each bottle has an aluminum seal around bottle neck. Do not use if any of these features are torn or damaged.

Principal Display Panel

FLONASE

ALLERGY RELIEF

Fluticasone Propionate Nasal Spray 50 mcg Per Spray Allergy Symptom Reliever (Glucocorticoid)*

Non-Drowsy Relief of:

Nasal congestion
Itchy, watery eyes
Itchy nose
Runny nose
Sneezing

FULL PRESCRIPTION STRENGTH

24 HOUR RELIEF

0.62 fl oz (18.2 mL)

144 METERED SPRAYS

*Fluticasone propionate is a steroid medicine known as a glucocorticoid.

Flonase Allergy 144 sprays
FLONASE ALLERGY RELIEF
fluticasone propionate spray, metered
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0576
Route of AdministrationNASAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FLUTICASONE PROPIONATE (UNII: O2GMZ0LF5W) (FLUTICASONE - UNII:CUT2W21N7U) FLUTICASONE PROPIONATE50 ug
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
WATER (UNII: 059QF0KO0R)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0576-011 in 1 CARTON06/30/2016
130 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2NDC:0135-0576-021 in 1 PACKAGE12/04/2014
260 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
3NDC:0135-0576-031 in 1 PACKAGE12/04/2014
3120 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
4NDC:0135-0576-043 in 1 PACKAGE01/07/2015
4120 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
5NDC:0135-0576-122 in 1 PACKAGE02/29/2016
5120 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
6NDC:0135-0576-141 in 1 PACKAGE11/17/2016
6144 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
7NDC:0135-0576-152 in 1 PACKAGE03/20/2017
7144 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
8NDC:0135-0576-163 in 1 PACKAGE03/20/2017
8144 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
9NDC:0135-0576-171 in 1 PACKAGE01/22/2019
972 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
10NDC:0135-0576-181 in 1 PACKAGE07/01/2021
1090 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA20543412/04/2014
Labeler - Haleon US Holdings LLC (079944263)