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Cymex Cream

Active Ingredient:
cetrimide , chlorocresol , Dimeticone 350 , urea
Company:  
Dexcel Pharma Ltd See contact details
ATC code: 
D02AX
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Last updated on emc: 13 May 2025

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Undesirable Effects Pharmacological Properties Interactions Posology Contraindications Excipients Storage precautions
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1. Name of the medicinal product

Cymex Cream

2. Qualitative and quantitative composition

Urea PhEur

1.0% w/w

Cetrimide PhEur

0.5% w/w

Dimeticone 350 PhEur

9.0% w/w

Chlorocresol PhEur

0.1% w/w

For a full list of excipients, see section 6.1.

3. Pharmaceutical form

Emollient White Cream

4. Clinical particulars
4.1 Therapeutic indications

For the application to cold sores and cracked lips.

4.2 Posology and method of administration

There are no special hazards associated with the use of cetrimide in specific patient groups. No special precautions or modified dosage requirements are, therefore, indicated for its use in infants, the elderly or during pregnancy or lactation. No hazardous drug interactions are considered likely.

Adults, elderly and children: apply sparingly every hour for the relief of cold sores and cracked lips.

Topical application.

4.3 Contraindications

Hypersensitivity to urea, cetrimide, dimeticone, chlorocresol or to any of the excipients listed in section 6.1.

4.4 Special warnings and precautions for use

Cymex Cream contains cetostearyl alcohol which may cause local skin reactions (e.g. contact dermatitis).

Keep out of the sight and reach of children.

For external use only.

If symptoms persist consult your doctor.

4.5 Interaction with other medicinal products and other forms of interaction

None known.

4.6 Pregnancy and lactation

Consult a doctor before use if pregnant or breast-feeding.

4.7 Effects on ability to drive and use machines

Not applicable.

4.8 Undesirable effects

None.

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 the Yellow Card Scheme; website: www.mhra.gov.uk/yellowcard

4.9 Overdose

Features

Symptoms are unlikely to arise after ingestion of this product. It is possible that nausea and vomiting or diarrhoea may occur.

Management

Gut decontamination or other specific management is unlikely to be required. Treat symptomatically. A small glass of milk or water may be helpful.

5. Pharmacological properties
5.1 Pharmacodynamic properties

ATC Code DO 2A X

Urea has keratolytic properties, Cetrimide is a quaternary ammonium disinfectant, Chlorocresol is a mild disinfectant while Dimeticone 350 acts as a water repellent.

5.2 Pharmacokinetic properties

Not applicable.

5.3 Preclinical safety data

No particular remarks.

6. Pharmaceutical particulars
6.1 List of excipients

Deionised Water

Liquid paraffin BP

Cetosteryl Alcohol BP

6.2 Incompatibilities

Not applicable.

6.3 Shelf life

36 months

6.4 Special precautions for storage

Store below 25ºC.

6.5 Nature and contents of container

5 g White Aluminium tubes with Elongated nozzles and HDPE caps. Internally lacquered.

6.6 Special precautions for disposal and other handling

See 4.2 Posology and Method of Administration.

7. Marketing authorisation holder

Dexcel®-Pharma Ltd.

7 Sopwith Way, Drayton Fields,

Daventry, Northamptonshire NN11 8PB

United Kingdom

8. Marketing authorisation number(s)

PL 14017/0309

9. Date of first authorisation/renewal of the authorisation

13th December 2007

10. Date of revision of the text

29/04/2024

Dexcel Pharma Ltd
Company image
Address
7, Sopwith Way, Drayton Fields, Daventry, Northamptonshire, NN11 8PB, UK
Telephone
+44 (0)1327 312 266
Fax
+44 (0)1327 312 262
Medical Information e-mail
[email protected]
Medical Information Direct Line
+44 (0) 1748 828 784
WWW
http://www.dexcelpharma.com
Out of Hours Telephone
+44 (0) 1748 828 784
E-mail
[email protected]