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-25% HYDROCUTAN Cream 0.25%, 20 g

HYDROCUTAN Cream 0.25%, 20 g

HYDROCUTAN Creme 0,25%

Manufacturers: DERMAPHARM AG

PZN: 01138717

Dosage: Creme

Content: 20 g

Reward Points: 38

Availability: In stock

$6.95

$5.20

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-25% HYDROCUTAN Cream 0.25%, 20 g
  • HYDROCUTAN Cream 0.25%, 20 g
  • HYDROCUTAN Cream 0.25%, 20 g
  • HYDROCUTAN Cream 0.25%, 20 g
  • HYDROCUTAN Cream 0.25%, 20 g

Instructions for use for HYDROCUTAN Cream 0.25%, 20 g

Application notes

The total dose should not be exceeded without consulting a doctor or pharmacist.

Type of application?
Apply the medicine to the person concerned. Wash your hands thoroughly after use. Avoid accidental contact with mucous membranes, eyes and open skin areas.

Duration of the application?
Without medical advice, you should not apply the medicine for more than 4 weeks. If you persevere or regularly recurring, you should see your doctor.

Overdose?
If the medicine is used as described, no overdose symptoms are known. With long -lasting use, among other things, steroid acne, expansion of small skin vessels, skin color change and skin dilution can occur. If in doubt, contact your doctor.

Forgot application?
Continue the application as normal at the next prescribed time (not with the double quantity).

In general, pay attention to a conscientious dosage especially in infants, toddlers and older people. If in doubt, ask your doctor or pharmacist about any effects or precautionary measures.

A dosage prescribed by the doctor may differ from the information on the package insert. Since the doctor coordinates you individually, you should therefore apply the medicine according to his instructions.
Dosage
Treatment start:
Children from 6 years and adults a sufficient amount 2-3 times a day regardless of the time of day
Follow -up treatment:
Children from 6 years and adults a sufficient amount 1 times a day regardless of the time of day, every 2-3 days interval

Application areas

- Skin inflammation, light shapes, e.g. B at:
   + Allergic skin disease

Mode of action

How does the ingredient of the medicine work?

The active ingredient is a related fabric to cortisone. Cortisone is a hormone that is also produced by the body.
In the event of injuries, the body's defense runs at full speed, a number of messenger substances and defense cells flock to the place of what is happening and destroyed the pathogens that have penetrated and caused by the violation of cell debris or blood clots. This work leads to inflammation in the affected area and associated with swelling, redness and ultimately pain. The active ingredient reduces these body's defense mechanisms, especially if - as with allergies - it is too exaggerated. It particularly has anti -inflammatory effect on the skin and eliminates itching, redness, swelling and pustules.

Composition

based on 1 g cream
2.5 mg hydrocortisone
+ Potassium sorbat
+ Glycerol (Mono/Di/Tri) Alkanoat (C12-C18)
+ Cetyl alcohol
+ Vaselin, white
+ Glycerol 85%
+ Glycerol monostataretat
+ Propylene glycol
+ Glycerolmono/Di (palmitat/stair)
+ Sodium stair
+ Citronic acid monohydrate
+ Sodium Citrat
+ Butylhydroxytoluole
+ Palmitoylascorbic acid
+ Water, cleaned

Contradictions

What speaks against an application?

- Hypersensitivity to the ingredients
- Virus infections of the skin, e.g. B.:
- Chickenpox
- Herpes infections
- Bacterial infections of the skin, such as:
- Skin tuberculosis
- Syphilis (LUES) (gender and skin disease)
- Acne
- Perioral dermatitis (acne -like inflammatory skin disease in the mouth area)
- Rosacea (inflammatory skin disease in the face area)
- Mushroom infections of the skin
- After a vaccination, skin reaction occurring

Which age group must be observed?
- Children under the age of 6: The medicine may onlye are used.

What about pregnancy and lactation?
- Pregnancy: Contact your doctor. Various considerations play a role in whether and how the medicine can be used during pregnancy.
- Still -time: Contact your doctor or pharmacist. He will check your special starting position and advise you accordingly whether and how you can continue with breastfeeding.

If the medicine has been prescribed to you despite a counter -notification, speak to your doctor or pharmacist. The therapeutic benefit can be higher than the risk of using the application.

Side effects

What adverse effects may occur?

For the medicine, only side effects are described that have so far only occurred in exceptional cases.

If you notice a disorder or change during treatment, contact your doctor or pharmacist.

For information at this point, side effects are taken into account that occurs in at least one of 1,000 patients treated.

Hints

What should you consider?
- Caution in corticoid allergy (e.g. cortisone)!
- Beware of allergy to ascorbic acid (vitamin C)!
- Antioxidants (e.g. butylhydroxyanisol, butylhydroxytoluole) can cause skin irritation (e.g. contact dermatitis), irritation of the eyes and mucous membranes.
- Emulgators (e.g. cetyl/stearl alcohol) can cause skin irritation (e.g. contact dermatitis).
- Solvent (e.g. propylene glycol, E 477) can cause skin irritation.
- Preservation materials (e.g. Sorbic acid and sorbate, E 200, E 201, E 202, E 203) can cause skin irritation (e.g. contact dermatitis).

Detailed instructions for HYDROCUTAN Cream 0.25%, 20 g

Field of use

  • This cream contains hydrocortisone, an active ingredient from the group of adrenal hormones (corticoids), which can be used to treat inflammatory and allergic skin diseases.
  • The cream is applied to treat inflammatory, allergic and itchy, often associated with blistering and crust formation (pruriginous) skin diseases, which appeal to external treatment with weakly effective corticoids.

Active ingredients / ingredients / ingredients

2.5 mg hydrocortisone
Butylhydroxytoluol HILDUFT (+)
Cetyl alcohol auxiliary material (+)
Citronic acid 1-water auxiliary material (+)
Glycerol (mono/di) (palmitat/stair) sodium stearate (95: 5) Hedge substance (+)
Glycerol (Mono/Di/Tri) Alkanoat (C12-C18) Hedge substance (+)
Glycerol 85% auxiliary material (+)
Glycerol monostataratotatel (+)
Sodium citrat auxiliary substance (+)
Sodium stair auxiliary material (+)
Palmitoyl ascorbic acid auxiliary material (+)
Propylen glycol auxiliary substance (+)
Vaselin, white auxiliary substance (+)
Water, cleaned auxiliary material (+)
Potassium sorbat auxiliary substance (+)

Contradictions

  • The medicine must not be used
    • if you are allergic to hydrocortisone or one of the other components of this medicine.
    • in children under 6 years without an express medical prescription
    • for special skin diseases (e.g. syphilis, skin tuberculosis)
    • in chickenpox
    • for skin reactions after vaccinations
    • in the case of bacterial or mushrooms from skin diseases
    • in certain skin diseases in the area of the face (rosacea and pink -like or perioral dermatitis) associated with reddening and/or noduling dermatitis)
    • on the eye and on mucous membranes
    • in the case of diseases with a disorder of the hypophysäär hypothalamic regulation (e.g. Cushing syndrome)

dosage

  • Always apply this medicine as described or exactly after the agreement made with your doctor or pharmacist. Ask your doctor or pharmacist if you are not sure.
  • The recommended dose is:
    • At the beginning of the treatment, you should apply the cream thinly 2 to 3 times a day. After improving the The clinical picture usually meets a one -time application/day or every 2 - 3 days.

 

  • Duration of the application
    • The duration of the application depends on the type, severity and the course of the disease
    • A long -term (longer than 4 weeks) or large area (more than 20 % of the body surface) Use of the cream should be avoided. This also applies to a more than 1 week treatment of more than 10 % of the body surface. Infants and toddlers under the age of 6 may only be treated with the preparation after express medical instructions and no longer than 3 weeks. Even after the clinical picture has subsided, the cream should be used for a few more days to avoid rebuilt.
    • To terminate the treatment, the frequency of application should be slowly reduced.
    • Please speak to your doctor or pharmacist if you have the impression that the effect of the cream is too strong or too weak.

 

  • If you have used a larger amount than you should
    • Reduce the dose or - if possible - put the medication after high -dosed and long -lasting (longer than four weeks).
    • In the case of long -term (longer than four weeks) large -scale (more than 20 % of the body surface), especially under final associations or on heavily pre -damaged skin, the active ingredient can be absorbed into the body and thus side effects such as: B. inhibition of the adrenal gland or M. Cushing (trunk fat, full moon face). In this case, see your doctor.

 

  • If you have forgotten the application
    • Do not apply the double dose if you have forgotten the previous application.

 

  • If you cancel the application
    • You could endanger the success of the treatment. Please speak to your doctor or pharmacist before you cancel the treatment.

 

  • If you have any further questions about the application of this medicine, please contact your doctor or pharmacist.

Taking

  • After careful cleaning of the skin, the cream is applied thinly to the diseased skin areas and slightly rubbed.

Patient information

  • Warnings and Precautions
    • Please speak to your doctor or pharmacist before using the preparation.
    • Special care in the application is required:
      • Long -term or large use of the cream should be avoided.
      • The cream must not be applied in an area of more than 1/10 of the body surface for more than 1 week.
      • Do not apply to open wounds!
      • The cream on the face should only be used with special caution.
      • When used in the face, make sure that the cream does not get in the eye (if the persons are predated, there is a risk of increasing the intraocular pressure).
      • If you see blurred vision or other visual disturbances, contact your doctor.
      • Do not apply to mucous membranes!
      • It is important to ensure that the use in infants and toddlers does not take place under occlusive conditions (airfall through diapers).

 

  • Wateriness and ability to operate machines
    • There is no experience with regard to the impairment of traffic and the ability to use machines.

Pregnancy

  • If you are pregnant or breastfeed, or if you suspect that you are pregnant or intend to become pregnant, ask your doctor or pharmacist for advice before using this drug.
  • Pregnancy
    • There is no sufficient data for using the preparation for pregnant women. Glucocorticoids showed fruit -damaging effects in animal experiments. Even in human fetuses, an increased risk of oral gap formations when using glucocorticoids during the first third of pregnancy is discussed. Animal studies have also shown that the administration of glucocorticsoids in therapeutic doses during pregnancy delay the growth of the unborn child and can contribute to the triggering of cardiovascular diseases and/or metabolic diseases in adulthood and a permanent change in behavior.
    • If you are pregnant, you may only apply the cream if your treating doctor considers this to be absolutely necessary. Please contact your doctor immediately.
  • Breastfeeding
    • The active ingredient contained in the cream changes to breast milk. With a large or long -term application, you should stop. A contact of the infant with the treated skin areas is to be avoided. Still mothers should not apply hydrocortisone in the area of the breast.

Hints

Read the package supplement and ask your doctor or pharmacist for risks and side effects.

Manufacturer:  DERMAPHARM AG, Lil-Dagover-Ring 7, 82031 Grünwald

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