Anhydrol Forte 20% w/v Cutaneous Solution

Product Information *

  • Company:

    Dermal Laboratories (Ireland) Ltd
  • Status:

    No Recent Update
  • Active Ingredients * :

    *Additional information is available upon request

  • Legal Category:

    Supply through pharmacy only

When a pharmaceutical company changes any document, a new version is published on medicines.ie. For each version, we show the dates it was published on medicines.ie and the reasons for change.

Updated on 17 December 2020

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:Supply through pharmacy only

Updated on 31 August 2018

Reasons for updating

  • File format updated to PDF

Legal category:Supply through pharmacy only

Free text change information supplied by the pharmaceutical company

File format updated to PDF

Updated on 14 July 2015

Reasons for updating

  • New PIL for new product

Updated on 14 July 2015

Reasons for updating

  • New SPC for new product

Legal category:Supply through pharmacy only

Updated on 14 July 2015

Reasons for updating

  • Change to Section 4.8 – Undesirable effects - how to report a side effect
  • Change to section 10 - Date of revision of the text
  • Improved electronic presentation

Legal category:Supply through pharmacy only

Free text change information supplied by the pharmaceutical company

In section 4.8 Undesirable effects, the following text has been added:

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important.  It allows continued monitoring of the benefit/risk balance of the medicinal product.  Healthcare professionals are asked to report any suspected adverse reactions via HPRA Pharmacovigilance, Earlsfort Terrace, IRL – Dublin 2; Tel: +353 1 6764971; Fax: +353 1 6762517.  Website: www.hpra.ie; E-mail: medsafety@hpra.ie.



In section 10 Date of revision of the text, the date has changed to "June 2015"

Updated on 14 July 2015

Reasons for updating

  • Change to date of revision
  • Addition of information on reporting a side effect.

Updated on 21 August 2014

Reasons for updating

  • Change to date of revision
  • Removal/change of distributor

Updated on 26 June 2009

Reasons for updating

  • Change due to user-testing of patient information

Updated on 29 August 2007

Reasons for updating

  • Change of trade or active ingredient name

Updated on 13 August 2007

Reasons for updating

  • Change to section 6.5 - Nature and contents of container

Legal category:Supply through pharmacy only

Free text change information supplied by the pharmaceutical company

Section 6.5 - Nature and contents of container: The text 'This is supplied as an original pack (OP)' has been removed.

Updated on 17 April 2007

Reasons for updating

  • Change to section 1 - Name of medicinal product

Legal category:Supply through pharmacy only

Free text change information supplied by the pharmaceutical company

Section 1 - Name of the Medicinal Product: The name has changed from "Anhydrol Forte" to "Anhydrol Forte 20% w/v Cutaneous Solution".

Updated on 03 September 2004

Reasons for updating

  • New PIL for medicines.ie

Updated on 12 June 2003

Reasons for updating

  • Change to section 6.3 - Shelf life
  • Change to section 9 - Date of renewal of authorisation

Legal category:Supply through pharmacy only

Updated on 09 June 2003

Reasons for updating

  • New SPC for medicines.ie

Legal category:Supply through pharmacy only