Allergy Relief by Rugby Laboratories, Inc. Drug Facts

Allergy Relief by

Drug Labeling and Warnings

Allergy Relief by is a Otc medication manufactured, distributed, or labeled by Rugby Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALLERGY RELIEF- fluticasone propionate spray, metered 
Rugby Laboratories, Inc.

----------

Drug Facts

Active Ingredient (in each spray)

Fluticasone propionate (glucocorticold) 50 mcg

Purpose

Allergy symptom reliever

Uses

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

• nasal congestion
• runny nose
• sneezing
• itchy nose
• itchy, watery eyes

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 (1-800-222-1222) right away.

Directions

• read the Quick Start Guide for how to:
  • prime the bottle
  • use the spray
  • 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

• TAMPER EVIDENT: Do not use if plastic sleeve is torn or broken under the cap and nozzle, each bottle has an aluminum seal around the bottle neck. Do not use if any any of these features are torn or damaged.
• 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 carton and enclosed insert. They contain important additional information.

Inactive ingredients

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

Questions or comments?

call 1-800-616-2471

Principal display panel

Compare to the active ingredient in Flonase®*

Full Prescription Strength

Fluticasone Propionate

Nasal Spray

(Glucocorticoid)< 50 mcg per spray

Allergy Symptom Reliever Nasal Spray

24 Hour

Relief of:

• Itchy, Watery Eyes
• Itchy Nose
• Nasal Congestion
• Sneezing
• Runny Nose

Non-drowsy

24-Hour Relief

Metered Sprays

FL OZ (mL)

*This product is not distributed by GlaxoSmithKline, owner of the registered trademark Flonase®.

Distributed by:

RUGBY LABORATORIES

Indianapolis, IN 46268

www.majorpharmaceuticals.com

Package label

RUGBY Allergy SymptomReliever Nasal Spray

ALLERGY RELIEF 
fluticasone propionate spray, metered

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0536-1373
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FLUTICASONE PROPIONATE (UNII: O2GMZ0LF5W) (FLUTICASONE - UNII:CUT2W21N7U)	FLUTICASONE PROPIONATE	50 ug

Inactive Ingredients
Ingredient Name	Strength
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 FORM (UNII: K679OBS311)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0536-1373-37	1 in 1 PACKAGE	09/15/2022	12/31/2024
1		60 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 0536-1373-38	1 in 1 PACKAGE	09/15/2022	12/31/2024
2		120 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA208024	09/15/2022	12/31/2024

Labeler - Rugby Laboratories, Inc. (079246066)

Revised: 10/2023

Document Id: 66ede09a-41a4-4e14-a007-31de53efec8f

34390-5

Set id: eaa08040-99f5-4ccc-82c5-469639f10601

Version: 4

Effective Time: 20231017