Nicam 4% w/w Gel
- Name:
Nicam 4% w/w Gel
- Company:
Dermal Laboratories Limited
- Active Ingredients:
- Legal Category:
Supply through pharmacy only
Patient Information Leaflet Patient Information Leaflet last updated on medicines.ie: 02/04/19

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Dermal Laboratories Limited

Company Products
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 2 April 2019 PIL
Reasons for updating
- Change to section 6 - date of revision
- Improved presentation of PIL
Updated on 2 April 2019 SmPC
Reasons for updating
- Change to section 6.1 - List of excipients
- Change to section 10 - Date of revision of the text
Legal category: Supply through pharmacy only
Updated on 31 August 2018 SmPC
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 26 March 2018 PIL
Reasons for updating
- New PIL for new product
Updated on 26 March 2018 PIL
Reasons for updating
- Change to section 6 - what the product contains
- Change to section 6 - date of revision
Updated on 7 December 2017 SmPC
Reasons for updating
- New SmPC for new product
Legal category: Supply through pharmacy only
Updated on 7 December 2017 SmPC
Reasons for updating
- Change to section 6.1 - List of excipients
- Change to section 10 - Date of revision of the text
- Improved presentation of SPC
Legal category: Supply through pharmacy only
Free text change information supplied by the pharmaceutical company
In section 10 (Date of revision of the text), the date has been changed to January 2017.
Updated on 4 March 2015 PIL
Reasons for updating
- Change to further information section
- Change to date of revision
- Addition of information on reporting a side effect.
- Removal/change of distributor
Updated on 17 February 2015 SmPC
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
Legal category: Supply through pharmacy only
Free text change information supplied by the pharmaceutical company
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 "February 2015" In section 10 Date of revision of the text, the date has changed to "February 2015"
Updated on 4 February 2014 PIL
Reasons for updating
- Change of manufacturer
Updated on 29 June 2009 PIL
Reasons for updating
- Change of inactive ingredient
Updated on 24 October 2008 SmPC
Reasons for updating
- Change to section 6.1 - List of excipients
- Change to section 10 - Date of revision of the text
Legal category: Supply through pharmacy only
Free text change information supplied by the pharmaceutical company
Updated on 22 July 2008 SmPC
Reasons for updating
- Change to section 1 - Name of medicinal product
- Change to section 9 - Date of renewal of authorisation
Legal category: Supply through pharmacy only
Free text change information supplied by the pharmaceutical company
Updated on 29 August 2007 PIL
Reasons for updating
- Change to further information section
Updated on 13 August 2007 SmPC
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
Updated on 21 July 2005 SmPC
Reasons for updating
- Change to section 6.3 - Shelf life
- Change to section 10 - Date of revision of the text
Legal category: Supply through pharmacy only
Updated on 8 September 2004 PIL
Reasons for updating
- New PIL for medicines.ie
Updated on 12 March 2004 SmPC
Reasons for updating
- Change to section 4.4 - Special warnings and precautions for use
- Change to section 4.8 - Undesirable effects
- Change to section 5.1 - Pharmacodynamic properties
- Change to section 5.3 - Preclinical safety data
- Change to section 6.1 - List of excipients
- Change to section 6.2 - Incompatibilities
- Change to section 6.6 - Special precautions for disposal and other handling
- Change to section 10 - Date of revision of the text
Legal category: Supply through pharmacy only
Updated on 13 June 2003 SmPC
Reasons for updating
- New SPC for medicines.ie
Legal category: Supply through pharmacy only