Description
Indications: Stimulation of the defensive system in cases of dermatitis, dermatosis, allergy, scleroderma, acne vulgaris, erythematodes, dermatomycosis, crusta lactea, condyloma, ecthyma, impetigo contagiosa, neurodermatitis, microsporosis, interdigital mycosis, decubitus, DupuytrenÕs contracture, loss of hair, naevi, QuinckeÕs oedema, elephantiasis.
Contraindications: Known allergy to ammonium bitumen sulphate.
Side effects: In rare cases, increased flow of saliva may occur after taking this medication. If this happens, the therapist should be consulted.
Interactions with other medication: None known.
Dosage: In acute disorders daily, otherwise 1 ampoule 3-1 times weekly or if necessary
Solution Composition:
Solution: 2.2 ml cont.: Cutis suis D8, Hepar suis D10, Splen suis D10, Placenta suis D10, Glandula suprarenalis suis D10, Funiculus umbilicalis suis D10, Thuja occidentalis D8, Galium aparine D6, Selenium D10, Thallium sulfuricum D13, Ignatia D6, Sulfur D10, Cortisonum aceticum D28, Urtica urens D4, Acidum phosphoricum D6, Calcium fluoratum D13, Mercurius solubilis Hahnemanni D13, Aesculus hippocastanum D6 Ichthyolum D28, Sanguinarinum nitricum D6, Ledum palustre D4, Arctium lappa D6, Acidum formicicum D198, Pyrogenium-Nosode D198, Acidum alpha-ketoglutaricum D10, Acidum fumaricum D10, Natrium diethyloxalaceticum D10 22 _l each.
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Cutis compositum N
Homeopathic medicinal product
Product status
Registered homeopathic medicinal product, therefore without indication of a therapeutic application.
If symptoms persist during use, medical advice should be sought.
Contraindications
Do not use if you are allergic to ichthyol (ammonium bituminosulfonate), any of the active substances,
or any of the other ingredients of this medicinal product.
Precautions for use
Ask your doctor for advice before using any medicinal product during pregnancy or breastfeeding.
This medicinal product contains less than 1 mmol (23 mg) sodium per ampoule, i.e. it is essentially “sodium-free”.
Interactions
The effect of a homeopathic medicinal product may be adversely influenced by generally harmful lifestyle factors
and by stimulants and luxury foods. Inform your doctor or pharmacist if you are using, have recently used,
or intend to use other medicinal products.
Dosage and method of administration
Unless otherwise prescribed: Use requires an individually tailored dosage by a therapist experienced in homeopathy.
For self-medication, only a single parenteral administration of 1–2 ml should be injected
intravenously (i.v.), intramuscularly (i.m.), or subcutaneously (s.c.).
To continue therapy, it is recommended to consult a therapist experienced in homeopathy.
Duration of use
As with all medicinal products, homeopathic medicinal products should not be used for prolonged periods without medical advice.
Side effects
Like all medicinal products, this medicinal product can have side effects, although not everybody gets them.
- Increased salivation may occur after use; if this happens, discontinue the product.
- Due to the homeopathic active ingredient Mercurius solubilis, allergic reactions may occur occasionally.
- When using homeopathic medicinal products, existing symptoms may temporarily worsen (initial aggravation). In this case, stop using the product and consult your doctor.
Instructions for opening the ampoule
Coloured dot facing upwards. Allow solution in the ampoule tip to flow downwards by tapping or shaking.
With the coloured dot facing upwards, pull the ampoule tip backwards to break it off.
Open the ampoule carefully and follow the instructions.
Composition
1 ampoule of 2.2 ml (= 2.2 g) contains:
- Cutis suis Dil. D8 (HAB, regulation 42a) – 22 mg
- Hepar suis Dil. D10 (HAB, regulation 42a) – 22 mg
- Splen suis Dil. D10 (HAB, regulation 42a) – 22 mg
- Placenta totalis suis Dil. D10 (HAB, regulation 42a) – 22 mg
- Glandula suprarenalis suis Dil. D10 (HAB, regulation 42a) – 22 mg
- Funiculus umbilicalis suis Dil. D10 (HAB, regulation 42a) – 22 mg
- Thuja occidentalis Dil. D8 – 22 mg
- Galium aparine Dil. D6 – 22 mg
- Selenium Dil. D10 – 22 mg
- Thallium sulfuricum Dil. D13 – 22 mg
- Strychnos ignatii Dil. D6 – 22 mg
- Sulfur Dil. D10 – 22 mg
- Cortisonum aceticum Dil. D28 (HAB, regulation 6) – 22 mg
- Urtica urens Dil. D4 – 22 mg
- Acidum phosphoricum Dil. D6 – 22 mg
- Calcium fluoratum Dil. D13 – 22 mg
- Mercurius solubilis Hahnemanni Dil. D13 – 22 mg
- Aesculus hippocastanum Dil. D6 – 22 mg
- Ammonium bituminosulfonicum Dil. D28 (HAB, regulation 5a; solution D1 with ethanol 15% m/m) – 22 mg
- Ledum palustre Dil. D4 – 22 mg
- Arctium Dil. D6 – 22 mg
- Acidum formicicum Dil. D198 – 22 mg
- Acidum alpha-ketoglutaricum Dil. D10 (HAB, regulation 5a; solution D1 with ethanol 43% m/m) – 22 mg
- Acidum fumaricum Dil. D10 (HAB, regulation 5a; solution D2 with ethanol 86% m/m) – 22 mg
- Natrium diethyloxalaceticum Dil. D10 (HAB, regulation 6) – 22 mg
Joint potentiation over the last 2 steps with water for injections.
Other ingredients: water for injections, sodium chloride.
Pharmaceutical form and pack size
Liquid dilution for injection.
Pack of 10 ampoules of 2.2 ml.
Clinic pack: 100 ampoules of 2.2 ml.
Storage
Keep medicines out of the reach of children. Do not use after the expiry date stated on the container and outer packaging.
No special storage conditions are required.
Manufacturer
Biologische Heilmittel Heel GmbH
Dr.-Reckeweg-Str. 2–4, 76532 Baden-Baden, Germany
Tel: +49 7221 501-00 | Fax: +49 7221 501-210
Email: info@heel.de
Pharmacy-only medicine. Registration No.: 37465.00.00
Leaflet information status: March 2023
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