IBUTOP Pain cream, 50 g
IBUTOP Schmerzcreme
Manufacturers: axicorp Pharma GmbH
PZN: 09750607
Dosage: Creme
Content: 50 g
Reward Points: 57
Availability: In stock
10.00€
5.14€
from German pharmacies to your address
Instructions for use for IBUTOP Pain cream, 50 g
ibutop® Pain cream
Active ingredient: ibuprofen.
Application areas:
Pain relieving and anti -inflammatory Medicines for rubbing into the skin. To the sole or supportive Treatment in muscle rheumatism, degenerative painful Joint diseases (arthrosis), inflammatory rheumatic diseases the joints and the spine, swelling or inflammation of the joints close to the joints Soft parts (e.g. bursa, tendon, tendon sheaths, ligaments and joint capsule), Shoulder stiffness, cross pain, lumbago, sports and accident injuries such as bruises, sprains, strains. Contains paraben (e219) and propylene glycol (E1520).
Read the package supplement and ask your doctor or pharmacist for risks and side effects.
axicorp Pharma GmbH, 61381 Friedrichsdorf.
As of July 2019.
Detailed instructions for IBUTOP Pain cream, 50 g
Field of use
- The drug is a pain -relieving and anti -inflammatory medicine for rubbing into the skin.
- Application areas
- For sole or supportive external treatment in muscle rheumatism, degenerative painful joint diseases (arthrosis), inflammatory rheumatic diseases of the joints and spine, swelling or inflammation of the soft soft tissues close to the joints (e.g. borders, tendons, straps and joint capsule), shoulder stiffness, Cross pain, lumbago, sports and accident injuries such as bruises, sprains, strains.
Mode of action
The special thing about ibutop pain cream (pack size: 50 g):
After the external application of ibutop pain cream (pack size: 50 g) on the skin, ibuprofen has an anti -inflammatory effect and relieves pain.
Active ingredients / ingredients / ingredients
Ibutop pain cream (pack size: 50 g) contains:
50 mg ibuprofen
Glycerol monostataratotatel (+)
Methyl 4-hydroxybenzoat, sodium salt auxiliary material (+)
Polyoxyethylene (100) monostatarat
Polyoxyethylene (1500) Monostetarat Home (+)
Propylen glycol auxiliary substance (+)
Triglyceride, medium -chain auxiliary material (+)
Water, cleaned auxiliary material (+)
Xanthan rubber auxiliary substance (+)
Contradictions
- The medicine must not be used
- if you are hypersensitive (allergic) against the active ingredient ibuprofen, the preservative methyl (4-hydroxybenzoat), sodium salt, propylene glycol, the other components of the drug or against other pain and rheumatism
- on open injuries, inflammation or infections of the skin, as well as on eczema or on mucous membranes
- in the last third of the pregnancy.
dosage
- Always apply the medicine exactly according to the instruction. Please ask your doctor or pharmacist if you are not quite sure.
- Unless otherwise prescribed by the doctor, the usual dose is:
- 3- 4 times a day
- Depending on the size of the painful area to be treated, a 4 - 10 cm long cream rank is required according to 2 - 5 g cream (100 - 250 mg ibuprofen). The maximum total daily dose is 20 g of cream according to 1000 mg ibuprofen.
- The practicing doctor will decide about the length of the treatments. As a rule, an application over 2 - 3 weeks is sufficient. The therapeutic benefit of an application beyond this period is not proven.
- Please speak to your doctor or pharmacist if you have the impression that the effect of the drug is too strong or too weak.
- If you have used a larger amount than you should
- If the recommended dosage is exceeded in the application the skin should be removed again and washed off with water. When using much too large quantities or accidental intake of the drug, the doctor must be notified.
- There is no specific antidote (antidote).
Taking
- Only for external use! Do not take!
- The medicine is applied to the skin and slightly rubbed into the skin. In the event of heavy bruises and compression, the use of an airtight association can be useful at the beginning of treatment. An increased penetration of the active ingredient through the skin can be achieved by using the ondophoresis (a special form of electrotherapy). The medicine must be applied under the cathode (minus pole). The current strength should be 0.1 - 0.5 mA per 5 cm² of electrode interface, the application time approx. 10 minutes.
Patient information
- The drug should not be used in children and adolescents under the age of 14, since there is no sufficient examinations for this age group.
- Patients suffering from asthma, hay fever, nasal mucosal swelling (so-called nasal polyps) or chronically obstructive respiratory diseases or chronic respiratory infections (particularly coupled with hay fever-like phenomena), and patients with hypersensitivity to pain and rheumatism are used when using the medicine (so-called Analgetics intolerance/analgesic asthma), local skin and mucosal swelling (so-called quincke-edema) or urticaria rather endangered than other patients.
- In these patients, the medicine may only be used under certain precautionary measures and direct medical control. The same applies to patients who also react hypersensitive to other substances, such as: B. with skin reactions, itching or nettle fever.
- It should be ensured that children with their hands do not get in touch with the skin areas grated with the medicine.
- In the event of complaints that last for more than 3 days, a doctor should be consulted.
- Wateriness and operating machines
- There are no special precautions required.
Pregnancy
- Pregnancy
- If pregnancy is determined during the application of the drug, the doctor must be notified. You can only use ibuprofen in the first and second thirds of pregnancy after consultation with your doctor. In the last third of pregnancy, the medicine must not be used due to the increased risk of complications for mother and child.
- Breastfeeding
- The active ingredient ibuprofen and its dismantling products pass into breast milk in only small quantities. Since adverse consequences for the infant have not yet become known, an interruption of breastfeeding will generally not be necessary if used briefly. However, a daily dose of 3 - 4 times with a 4 - 10 cm long cream rank should not be exceeded and an early weaning should be considered if used for a long time. In order to avoid recording by the infant, breastfeeding may not apply the medicine in the chest area.
Hints
- The drug should not be used in children and adolescents under the age of 14, since there is no sufficient examinations for this age group.
- Patients who have asthma, hay fever, nasal mucosal swelling (so -called. Nasal polyps) or chronically obstructive respiratory diseases or chronic respiratory infections (particularly coupled with hay fever-like phenomena), and patients with hypersensitivity to pain and rheumatism of all kinds are when using the medicine (so-called analgesics/analgesic asthma), local skin And mucosal swelling (so-called quincke-edema) or urticaria endangered rather than other patients.
- In these patients, the medicine may only apply under certain precautionary measures and direct medical controlbe turned. The same applies to patients who also react hypersensitive to other substances, such as: B. with skin reactions, itching or nettle fever.
- It should be ensured that children with their hands do not get in touch with the skin areas grated with the medicine.
- In the event of complaints that last for more than 3 days, a doctor should be consulted.
- Wateriness and operating machines
- There are no special precautions required.
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