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Dermovit F

Dermovit F

About the medicine

How to use Dermovit F

INFORMATION PLACED ON OUTER PACKAGING

{Carton box for PE 30 g box}

1. NAME OF THE MEDICINAL PRODUCT

DERMOVIT F25 mg/g, ointment
(Vitaminum F)

2. LIST OF ACTIVE SUBSTANCES

1 g of ointment contains: active substance - 25 mg of vitamin F

3. LIST OF EXCIPIENTS

Excipients: anhydrous euceryne, purified water, lavender oil.

4. PHARMACEUTICAL FORM AND CONTENT OF THE PACKAGING

ointment
30 g - EAN UCC Code: 5909990667598

5. METHOD AND ROUTE OF ADMINISTRATION

Administration on the skin.

6. WARNING ABOUT STORAGE OF THE MEDICINAL PRODUCT

IN A PLACE INVISIBLE AND INACCESSIBLE TO CHILDREN

The medicine should be stored in a place invisible and inaccessible to children.

7. OTHER SPECIAL WARNINGS, IF NECESSARY

8. EXPIRY DATE

Expiry date:
The medicine should not be used after the expiry date stated on the packaging.

9. STORAGE CONDITIONS

Store at a temperature below 25°C. Store in the original, tightly closed
packaging, to protect from light.

10. SPECIAL PRECAUTIONS FOR DISPOSAL OF UNUSED

MEDICINAL PRODUCT OR WASTE ARISING FROM IT, IF APPROPRIATE

MEASURES

11. NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER

Marketing authorisation holder:
LABORATORY OF PHARMACEUTICAL PRODUCTS "COEL" S.J.
EZM KONSTANTY
ul. Wł. Żeleńskiego 45, 31-353 Kraków.

12. MARKETING AUTHORISATION NUMBER

Marketing authorisation number: R\2039

13. BATCH NUMBER

Batch number:

14. GENERAL CATEGORY OF AVAILABILITY

OTC - Medicinal product available without prescription.

15. INSTRUCTIONS FOR USE

16. INFORMATION PROVIDED IN BRAILLE SYSTEM

dermovit F coel

17. OTHER

Indications for use:
Ointment for topical use on the skin in children and adults with trophic skin changes,
psoriasis, eczematous dermatitis, bedsores and burns.
Dosage and method of administration:
Cleaned skin surface should be smeared with a thin layer of ointment once or twice a day. In
acute disease conditions, the skin can be smeared several times a day.
Contraindications:
The medicine should not be used:

  • in hypersensitivity to vitamin F or to any of the components of the medicine;
  • in the eyes and on mucous membranes.

Pregnancy and breastfeeding:
Before using the medicine, consult a doctor.
There are no data on the use of the medicine in pregnant and breastfeeding women.
Undesirable effects:
Allergic reactions and contact dermatitis may occur.
Reporting undesirable effects
If any undesirable effects occur, including any effects not listed in the leaflet, inform your doctor, pharmacist or nurse.
Undesirable effects can be reported directly to the Department of Monitoring of Undesirable Effects of Medicinal Products, Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: +48 22 49 21 301, fax: +48 22 49 21 309, e-mail: ndl@urpl.gov.pl.
Reporting undesirable effects allows for the collection of more information on the safety of the medicine.

Talk to a doctor online

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