FLUTICASONE PROPIONATE ALLERGY RELIEF- fluticasone propionate spray, metered 
GLENMARK THERAPEUTICS INC., USA

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Drug Facts

Active Ingredient (in each spray)

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

Purpose

Allergy symptom reliever

Uses

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.

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

Other information

•
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, phenylethyl alcohol, polysorbate 80, water for injection, sodium carboxymethylcellulose

Questions or comments?

Call toll-free weekdays 9 AM to 6 PM EST at 1 (888) 721-7115.

Generic Section

Fluticasone Propionate Nasal Spray Allergy Relief helps relieve a broad range of uncomfortable symptoms like congestion and itchy eyes.

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

Outdoor allergens

Animal allergens

Indoor allergens

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

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

Principal Display Panel

FLUTICASONE PROPIONATE NASAL SPRAY, USP

50 mcg per spray

ALLERGY SYMPTOM RELIEVER

(Glucocorticoid)*

Non-Drowsy Relief of:

•
Nasal congestion
•
Itchy, watery eyes
•
Itchy nose
•
Runny nose
•
Sneezing

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

FULL PRESCRIPTION STRENGTH

24 HOUR ALLERGY RELIEF

120 METERED SPRAYS

0.54 fl oz (15.8 mL)

carton120sprays
FLUTICASONE PROPIONATE  ALLERGY RELIEF
fluticasone propionate spray, metered
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72657-159
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)  
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)  
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:72657-159-601 in 1 CARTON03/16/2026
160 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2NDC:72657-159-121 in 1 CARTON03/16/2026
2120 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
3NDC:72657-159-242 in 1 CARTON03/16/2026
3120 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
4NDC:72657-159-363 in 1 CARTON03/16/2026
4120 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
5NDC:72657-159-141 in 1 CARTON03/16/2026
5144 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
6NDC:72657-159-282 in 1 CARTON03/16/2026
6144 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
7NDC:72657-159-423 in 1 CARTON03/16/2026
7144 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
8NDC:72657-159-721 in 1 CARTON03/16/2026
872 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
9NDC:72657-159-484 in 1 CARTON03/16/2026
9120 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
ANDAANDA21874203/16/2026
Labeler - GLENMARK THERAPEUTICS INC., USA (969085666)
Establishment
NameAddressID/FEIBusiness Operations
Glenmark Pharmaceuticals Limited650565703MANUFACTURE(72657-159)

Revised: 5/2026
Document Id: 282e11b5-3962-4e31-87c0-18163fa04f92
Set id: 5494106f-6792-409e-b63f-b63b98140959
Version: 2
Effective Time: 20260505
 
GLENMARK THERAPEUTICS INC., USA