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JOD-WUNDSALBE STADA 100 mg/g, 20 g

Name: JOD-WUNDSALBE STADA 100 mg/g, 20 g
Brand: STADA Consumer Health Deutschland GmbH
SKU: 17483089
Price: 5.54 USD
Availability: InStock

JOD-WUNDSALBE STADA 100 mg/g 20 g Salbe

Manufacturers: STADA Consumer Health Deutschland GmbH

PZN: 17483089

Dosage: Salbe

Content: 20 g

Reward Points: 46

Availability: In stock

~~5.39€~~

4.62€

20 g 100 g

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Instructions for use for JOD-WUNDSALBE STADA 100 mg/g, 20 g

Instructions for use

How to use?
Apply the medicine to the affected area(s) of skin. The area(s) treated with the medicine can be covered with a bandage.

Duration of use?
Use should be continued until symptoms subside. If symptoms recur after treatment, please consult your doctor.

Overdose?
If the medicine is accidentally ingested, overdose symptoms may include abdominal pain, nausea, vomiting, diarrhea, headache, cramps, and even collapse. If an overdose is suspected, consult a doctor immediately.

In general, pay careful attention to the dosage, especially for infants, small children, and the elderly. If in doubt, ask your doctor or pharmacist about any possible side effects or precautions.

Dosage prescribed by a doctor may differ from the information in the package leaflet. Since the doctor adjusts the dosage individually, you should therefore use the medicine according to his or her instructions.

Dosage

For application to the skin:

Infants from 6 months, children, adolescents, and adults

a sufficient amount

once or several times daily

regardless of the time of day

Indications

- Bedsores

- Ulcers on the leg or foot due to circulatory disorders (ulcus cruris)

- Wounds (superficial)

- Burns

- infected skin disease (dermatosis)

- superinfected skin disease (dermatosis)

Mode of action

How does the active ingredient in the medicine work?

Iodine is bound to carrier substances to reduce germs (disinfect) and to support wound healing. Iodine is effective against a wide range of pathogens, such as bacteria, viruses, and fungi.

Composition

based on 1 g of ointment

100 mg povidone iodine

10 mg iodine

+ Macrogol 400

+ Macrogol 4000

+ Purified water

Contraindications

What are the contraindications?

Always:
- Hypersensitivity to the ingredients
- Hyperthyroidism
- Thyroid disease, including a history of itching
- Dermatitis herpetiformis (immune disease with an itchy rash with blisters)
- Upcoming or recently completed radioiodine therapy

In certain circumstances - consult your doctor or pharmacist:
- Benign goiter (struma)
- Thyroid autonomy (certain form of hyperthyroidism)

Which age group should be considered?
- Premature babies: This medicine must not be used.
- Infants under 6 months: This medicine should only be used after consultation with a doctor or under medical supervision.

What about pregnancy and breastfeeding?
- Pregnancy: Consult your doctor. Various considerations play a role in whether and how the medicine can be used during pregnancy.
- Breastfeeding: Consult your doctor or pharmacist. They will assess your specific situation and advise you accordingly on whether and how you can continue breastfeeding.

If you have been prescribed the medicine despite a contraindication, talk to your doctor or pharmacist. The therapeutic benefit may outweigh the risk associated with use in the presence of a contraindication.

Side effects

What adverse effects can occur?

Always:
- Hypersensitivity
- Acute severe allergic reaction affecting several or all areas of the body (anaphylaxis)
- Circulatory failure due to an allergic reaction (anaphylactic shock)
- Spontaneous swelling of the (mucous) skin (angioedema)
- Hyperthyroidism due to excessive iodine intake
- Hypersensitivity reactions of the skin, such as:
- Contact dermatitis (allergic skin reactions that only occur with repeated use)
- Itching
- Reddening of the skin
- Blistering

Under certain circumstances, with the ingestion of larger amounts of the active ingredient, e.g., in the case of burns and long-term use:
- Disturbance of the Salt balance
- Altered concentration of water-binding substances (osmotic) in the blood
- Impaired kidney function
- Metabolic disorder with hyperacidity of the blood (metabolic acidosis)

If you notice any discomfort or changes during treatment, contact your doctor or pharmacist.

For the information provided here, side effects that occur in at least one in 1,000 treated patients are primarily considered.

Notes

What should you be aware of?
- There may be interactions with certain medications. Therefore, you should generally inform your doctor or pharmacist about any other medication you are already using before starting treatment with a new medication. This also applies to medications you buy yourself, use only occasionally, or have used for some time.

Detailed instructions for JOD-WUNDSALBE STADA 100 mg/g, 20 g

Iodine Wound Ointment STADA^® 100 mg/g Ointment

Active ingredient:
Povidone Iodine.

For repeated, limited-term use: as an antiseptic for damaged skin, e.g., decubitus ulcers (pressure sores), leg ulcers (lower leg ulcers), superficial wounds and burns, and infected and superinfected skin diseases.

For information on risks and side effects, read the package insert and ask your doctor or pharmacist.
STADA Consumer Health Deutschland GmbH, Stadastraße 2–18, 61118 Bad Vilbel
As of: November 2020

EINFACHE ANWENDUNG BEI KLEINEN WUNDEN UND VERLETZUNGEN
For minor wounds and injuries, the body initiates its own repair mechanism. Wound healing is divided into three stages:
1. Blood Coagulation:
The wound usually closes quickly, so that the scab prevents blood loss and the penetration of bacteria.
2. Granulation:
The healing process begins beneath the scab. A layer of granulation tissue forms. During this stage, the wound may feel tight and possibly itchy.
3. Tissue Regeneration:
After phase 2, the regeneration of the original tissue begins.

ANWENDUNGSEMPFEHLUNG
Unless otherwise prescribed by a doctor, the usual application is
Apply Iodine Wound Ointment STADA^® evenly to the injured area once or several times daily. If necessary, a bandage can be applied afterward. The brown color of Iodine Wound Ointment STADA^® is a property of the product and indicates its effectiveness. Extensive discoloration indicates that the product's effectiveness has been exhausted.

Duration of Use
The use of Iodine Wound Ointment STADA^® should be continued as long as signs of inflammation persist. If your symptoms have not improved after several days (2 to 5 days) of regular use of Iodine Wound Ointment STADA^® , or if symptoms recur after treatment, please consult your doctor.

What is the composition of Iodine Wound Ointment STADA^® 100 mg/g ointment and what packages are available?
The active ingredient is povidone-iodine
100 g of ointment contains 10 g povidone-iodine, average molecular weight 40,000, with a 10% available iodine content.

The other ingredients are:
Macrogol 400, Macrogol 4000, purified water.

What Iodine Wound Ointment STADA^® looks like and contents of the package Reddish-brown ointment.

Iodine Wound Ointment STADA^® is available in 20 g and 100 g tubes.

HÄUFIGE FRAGEN & ANTWORTEN

Does taking Iodine Wound Ointment STADA^® 100 mg/g affect the ability to drive and operate machinery?
No effects on the ability to drive and operate machinery have been reported to date.

Can pregnant or breastfeeding women take Iodine Wound Ointment STADA^® 100 mg/g?
If you are pregnant or breastfeeding, suspect you may be pregnant, or are planning to become pregnant, consult your doctor or pharmacist before using this medicine.

During pregnancy and breastfeeding, Iodine Wound Ointment STADA^® should only be used on the express instructions of a doctor and in a very limited manner. In this case, monitoring of the child's thyroid function is necessary. Accidental ingestion of Iodine Wound Ointment STADA^® by the infant through the mouth at the breast of the nursing mother must be avoided at all costs.