Rhinolast 140 micrograms per Spray, Nasal Spray

*
Pharmacy Only: Prescription
  • Company:

    Mylan IRE Healthcare Ltd
  • Status:

    No Recent Update
  • Legal Category:

    Product subject to medical prescription which may be renewed (B)
  • Active Ingredient(s):

    *Additional information is available within the SPC or upon request to the company

Updated on 24 February 2022

File name

ie-pl-rhinolast-excipient name-clean.pdf

Reasons for updating

  • Change to section 4 - possible side effects
  • Change to section 6 - date of revision

Updated on 24 February 2022

File name

ie-spc-rhinolast-excipient name-clean.pdf

Reasons for updating

  • Change to section 4.8 - Undesirable effects
  • Change to section 6.1 - List of excipients
  • Change to section 10 - Date of revision of the text

Legal category:Product subject to medical prescription which may be renewed (B)

Updated on 27 April 2021

File name

ie-pl-rhinolast-clean (delete MMC).pdf

Reasons for updating

  • Change to section 6 - manufacturer
  • Change to section 6 - date of revision

Updated on 16 October 2018

File name

ie-pl-rhinolast-clean-mahtransfer.pdf

Reasons for updating

  • New PIL for new product

Updated on 16 October 2018

File name

ie-spc-rhinolast-clean-mahtransfer.pdf

Reasons for updating

  • Change to section 7 - Marketing authorisation holder
  • Change to section 8 - Marketing authorisation number(s)
  • Change to section 10 - Date of revision of the text

Legal category:Product subject to medical prescription which may be renewed (B)

Updated on 09 March 2015

Reasons for updating

  • New SPC for new product

Legal category:Product subject to medical prescription which may be renewed (B)

Updated on 09 March 2015

Reasons for updating

  • Change to section 4.6 - Pregnancy and lactation
  • Change to Section 4.8 – Undesirable effects - how to report a side effect
  • Change to section 10 - Date of revision of the text

Legal category:Product subject to medical prescription which may be renewed (B)

Free text change information supplied by the pharmaceutical company

In section 4.6: Subheading has been expanded to include fertility

In section 4.8: the ADR statement was added

In section 10: the date of revision has changed

Updated on 09 March 2015

Reasons for updating

  • Change to section 4.6 - Pregnancy and lactation
  • Change to Section 4.8 – Undesirable effects - how to report a side effect
  • Change to section 10 - Date of revision of the text

Free text change information supplied by the pharmaceutical company

In section 4.6: Subheading has been expanded to include fertility

In section 4.8: the ADR statement was added

In section 10: the date of revision has changed

Updated on 07 June 2012

Reasons for updating

  • Change to section 2 - Qualitative and quantitative composition
  • Change to section 9 - Date of renewal of authorisation
  • Change to section 10 - Date of revision of the text

Legal category:Product subject to medical prescription which may be renewed (B)

Free text change information supplied by the pharmaceutical company

In section 2; the following text has been added... for a full list of excipients
In section 9; the renewal date has been revised
In section 10; the revision date is now May 2012

Updated on 07 June 2012

Reasons for updating

  • Change to section 2 - Qualitative and quantitative composition
  • Change to section 9 - Date of renewal of authorisation
  • Change to section 10 - Date of revision of the text

Free text change information supplied by the pharmaceutical company

In section 2; the following text has been added... for a full list of excipients
In section 9; the renewal date has been revised
In section 10; the revision date is now May 2012

Updated on 08 April 2011

Reasons for updating

  • New SPC for medicines.ie

Legal category:Product subject to medical prescription which may be renewed (B)

Free text change information supplied by the pharmaceutical company

None provided

Updated on 08 April 2011

Reasons for updating

  • New SPC for medicines.ie

Free text change information supplied by the pharmaceutical company

None provided