Beeovita
Omida Rubiderm N Ointment Tb 50 g
Omida Rubiderm N Ointment Tb 50 g

Omida Rubiderm N Ointment Tb 50 g

Omida Rubiderm N Salbe Tb 50 g

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  • Availability: In stock
  • Distributor: OMIDA AG
  • Product Code: 1636007
  • ATC-code D11AZ
  • EAN 7680533240109
Amount in a pack. 1
Storage temp. min 15 / max 25 ℃

Ingredients:

Psoriasis

Description

Swissmedic-approved patient information

OMIDA® Rubiderm-N

Omida AG

Homeopathic medicinal product

AMZV

When is OMIDA Rubiderm-N used?

According to the homeopathic drug picture can OMIDA® Rubiderm-N at

-dry, scaly and eczematous skin rashes

-psoriasis, on medical prescription, especially between the acute episodes

are applied.

What should you pay attention to?

If your doctor has prescribed other medicines for you, ask your doctor, pharmacist or druggist Druggist whether OMIDA® Rubiderm-N can be used at the same time.

When should OMIDA Rubiderm-N not be used or only with caution?

OMIDA® Rubiderm-N must not be used on open and bacterially infected wounds or if there is a known allergy to an active ingredient or a component of

Ointment base.

Tell your doctor, pharmacist or druggist if you

-suffering from other diseases,

have allergies or

-Take other medicines (including those you bought yourself!) or use them externally!

Can OMIDA Rubiderm-N be used during pregnancy or breastfeeding?

OMIDA® Rubiderm-N N must not be used during pregnancy and lactation.

How do you use OMIDA Rubiderm-N?

Unless otherwise prescribed by the doctor, 2-3 times for long-term therapy Apply thinly to the affected areas of skin every day and massage in lightly or apply an ointment bandage, e.g. at night.

Follow the dosage given in the package leaflet or as prescribed by your doctor.

If the desired improvement does not occur during the treatment of a small child/child, a doctor should be consulted with them.

If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.

What side effects can OMIDA Rubiderm-N have?

For OMIDA® Rubiderm-N have so far been used as intended Use no side effects have been observed.

If you nevertheless observe side effects, inform your doctor, pharmacist or druggist.

When using homeopathic medicines, the symptoms can temporarily worsen (initial aggravation). If the deterioration persists, discontinue OMIDA® Rubiderm-N and inform your doctor, pharmacist or druggist.

What else needs to be considered?

The medicinal product may only be used up to the date marked ‹‹EXP›› on the container.

Keep the medicine out of the reach of children and at room temperature (15-25°C).

Your doctor, pharmacist or druggist can provide you with further information.

What does OMIDA Rubiderm-N contain?

1 g ointment contains:

Mahonia aquifolium (mahonia) TM 100 mg.

This preparation contains additional excipients: benzyl alcohol (preservative), cetostearyl alcohol, thick paraffin, octyldodecanol, white vaseline, water.

Approval number

53324 (Swissmedic)

Where can you get OMIDA Rubiderm-N? What packs are available?

In pharmacies and drugstores, without a doctor's prescription.

Tubes of 50 g.

Authorization holder

Omida AG, Erlistrasse 2, 6403 Küssnacht am Rigi

This leaflet was last checked by the drug authority (Swissmedic) in March 2009.

Swissmedic-approved patient information

OMIDA® Rubiderm-N

Omida AG

Homeopathic medicinal product

AMZV

When is OMIDA Rubiderm-N used?

According to the homeopathic drug picture can OMIDA® Rubiderm-N at

-dry, scaly and eczematous skin rashes

-psoriasis, on medical prescription, especially between the acute episodes

are applied.

What should you pay attention to?

If your doctor has prescribed other medicines for you, ask your doctor, pharmacist or druggist Druggist whether OMIDA® Rubiderm-N can be used at the same time.

When should OMIDA Rubiderm-N not be used or only with caution?

OMIDA® Rubiderm-N must not be used on open and bacterially infected wounds or if there is a known allergy to an active ingredient or a component of

Ointment base.

Tell your doctor, pharmacist or druggist if you

-suffering from other diseases,

have allergies or

-Take other medicines (including those you bought yourself!) or use them externally!

Can OMIDA Rubiderm-N be used during pregnancy or breastfeeding?

OMIDA® Rubiderm-N N must not be used during pregnancy and lactation.

How do you use OMIDA Rubiderm-N?

If not otherwise prescribed by the doctor, 2-3 times for long-term therapy Apply thinly to the affected areas of skin every day and massage in lightly or apply an ointment bandage, e.g. at night.

Follow the dosage given in the package leaflet or as prescribed by your doctor.

If the desired improvement does not occur during the treatment of a small child/child, a doctor should be consulted with them.

If you think the medicine is too weak or too strong, talk to your doctor, pharmacist or druggist.

What side effects can OMIDA Rubiderm-N have?

For OMIDA® Rubiderm-N have so far been used as intended Use no side effects have been observed.

If you nevertheless observe side effects, inform your doctor, pharmacist or druggist.

When using homeopathic medicines, the symptoms can temporarily worsen (initial aggravation). If the deterioration persists, discontinue OMIDA® Rubiderm-N and inform your doctor, pharmacist or druggist.

What else needs to be considered?

The medicinal product may only be used up to the date marked ‹‹EXP›› on the container.

Keep the medicine out of the reach of children and at room temperature (15-25°C).

Your doctor, pharmacist or druggist can provide you with further information.

What does OMIDA Rubiderm-N contain?

1 g ointment contains:

Mahonia aquifolium (mahonia) TM 100 mg.

This preparation contains additional excipients: benzyl alcohol (preservative), cetostearyl alcohol, thick paraffin, octyldodecanol, white vaseline, water.

Approval number

53324 (Swissmedic)

Where can you get OMIDA Rubiderm-N? What packs are available?

In pharmacies and drugstores, without a doctor's prescription.

Tubes of 50 g.

Authorization holder

Omida AG, Erlistrasse 2, 6403 Küssnacht am Rigi

This leaflet was last checked by the drug authority (Swissmedic) in March 2009.

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