Label: FLONASE ALLERGY RELIEF- fluticasone propionate spray, metered
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- NDC Code(s): 70518-1223-0, 70518-1223-1
- Packager: REMEDYREPACK INC.
- This is a repackaged label.
- Source NDC Code(s): 0135-0576
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated April 15, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient (in each spray)
- Purpose
- Uses
-
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 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
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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
- read the Quick Start Guide for how to:
- Other information
- Inactive ingredients
- Questions or comments?
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PRINCIPAL DISPLAY PANEL
DRUG: FLONASEALLERGY RELIEF ALLERGY RELIEF
GENERIC: fluticasone propionate
DOSAGE: SPRAY, METERED
ADMINSTRATION: NASAL
NDC: 70518-1223-0
NDC: 70518-1223-1
PACKAGING: 120 in 1 BOTTLE
OUTER PACKAGING: 1 in 1 PACKAGE
PACKAGING: 144 in 1 BOTTLE
OUTER PACKAGING: 1 in 1 PACKAGE
ACTIVE INGREDIENT(S):
- FLUTICASONE PROPIONATE 50ug in 1
INACTIVE INGREDIENT(S):
- BENZALKONIUM CHLORIDE
- DEXTROSE, UNSPECIFIED FORM
- MICROCRYSTALLINE CELLULOSE
- PHENYLETHYL ALCOHOL
- POLYSORBATE 80
- WATER
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM
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INGREDIENTS AND APPEARANCE
FLONASE ALLERGY RELIEF
fluticasone propionate spray, meteredProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70518-1223(NDC:0135-0576) 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:70518-1223-0 1 in 1 PACKAGE 05/25/2018 06/08/2018 1 120 in 1 BOTTLE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.) 2 NDC:70518-1223-1 1 in 1 PACKAGE 04/15/2021 2 144 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 NDA NDA205434 05/25/2018 Labeler - REMEDYREPACK INC. (829572556)