Product information

From Health Canada

The product monograph is developed by a drug sponsor according to guidelines published by Health Canada that provide direction on the content and format. The veterinary labelling is developed by the drug sponsor according to the Food and Drug Regulations. While Health Canada reviews the product monograph or the veterinary labelling as part of the drug review process, it remains the responsibility of the drug sponsor to ensure that the product monograph or the veterinary labelling is complete and accurate.

Current status:

Marketed

Current status date:

2017-02-01

Original market date: See footnote 1

2017-02-01

Product name:

FLONASE ALLERGY RELIEF

Description:

SUSPENSION

Help on accessing alternative formats, such as Portable Document Format (PDF), Microsoft Word and PowerPoint (PPT) files, can be obtained in the alternate format help section.

DIN:

02248307

Product Monograph/Veterinary Labelling:

Date: 2019-07-22 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company:

GLAXOSMITHKLINE CONSUMER HEALTHCARE ULC
450 55 Standish Court
Mississauga
Ontario
Canada L5R 4B2

Class:

Human

Dosage form(s):

Spray, Metered Dose

Route(s) of administration:

Nasal

Number of active ingredient(s):

1

Schedule(s):

OTC

 

American Hospital Formulary Service (AHFS): See footnote 3

52:08.00 

Anatomical Therapeutic Chemical (ATC): See footnote 4

R01AD08 FLUTICASONE

Active ingredient group (AIG) number:See footnote5

0124685001

List of active ingredient(s)
Active ingredient(s) Strength
FLUTICASONE PROPIONATE 50 MCG / ACT
Version 4.0.2
Date modified: