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Proprietary name and dosage form:

ZEEL®T TABLETS

Composition: Cartilago suis D4 0,3 mg; Funiculus umbilicalis suis D4 0,3 mg; Embryo suis D4 0,3 mg; Placenta suis D4 0,3 mg;Toxicodendron quercifolius D2 0,54 mg; Arnica Montana D1 0,6 mg; Solanum dulcamara D2 0,15 mg; Symphytum officinale D8  0,15 mg; Sanguinaria Canadensis D3 0,45 mg; Sulfur D6 0,54 mg; Nadidum D6 0,03 mg; Coenzymum A D6 0,03 mg; Natrium diethyloxalaceticum D6 0,03 mg; Acidum alpha-liponicum D6 0,03 mg; Acidum silicicum D6 3 mg.One tablet contains approx. 300 mg lactose.
Indications: This medicine is prepared in accordance with homeopathic principles and is proposed for use in arthrosis (in particular gonarthrosis); polyarthrosis, spondylarthrosis, scapulohumeral periarthritis.
Contraindications: Hypersensitivity to botanicals of the Compositae family or the genus Rhus of the Anacardiaceae family.
Zeel® T should be used only in consultation with a physician in cases of active or prior liver disease and/or if used in combination with hepatotoxic drugs.
Because it contains bloodroot (Sanguinaria canadensis), Zeel® T should not be used during pregnancy and lactation.
Warnings: This preparation contains natural lactose. Although the quantity of lactose present is probably not sufficient to cause discomfort, a health professional should be consulted in strong cases of lactose intolerance. A temporary aggravation of the existing symptoms is possible after taking a homeopathic preparation.
Interactions: No interactions studies have been performed.
Pregnancy and lactation: If you are pregnant or breast feeding your baby please consult your doctor, pharmacist or other health care professional for advice before taking this medicine.
Dosage and directions for use: Adults: In general, 1 tablet to be dissolved in the mouth 3-5 times daily.Always tell your health care professional if you are taking any other medicine.  In the event of over dosage, consult your doctor or pharmacist.  If neither is available, contact the nearest poison control centre.
Side Effects and Special Precautions: Side Effects
During treatment with medications containing sanguinarin, elevated levels of liver enzymes (transaminases) and bilirubin have been observed in individual cases, to the point of drug-induced hepatitis and jaundice. These symptoms abated when treatment was discontinued.
In very rare cases, gastrointestinal symptoms or skin reactions may appear as late as several days after using the medication.Not all side effects reported for this medicine are included in this leaflet.  Should your general health worsen or if you experience untoward effects while taking this medicine, please consult your doctor, pharmacist or other health care professional for advice.
Registration number: To be allocated by Council.
Disclaimer: This medicine has not been evaluated by the Medicines Control Council. This medicine is not intended to diagnose, treat, cure or prevent any disease.

Proprietary name and dosage form:

ZEEL®T OINTMENT

Composition: 100 g ointment cont.:  Cartilago suis D2 0,001 g; Funiculus umbilicalis suis D2 0,001 g; Embryo suis D2 0,001 g; Placenta suis D2 0,001 g; Rhus toxicodendron D2 0,27 g; Arnica Montana D2 0,30 g; Solanum dulcamara D2 0,075 g; Symphytum officinale D8 0,75 g; Sanguinaria Canadensis   D2 0,225 g; Sulfur D6 0,27 g; Nadidum D6 0,01 g; Coenzymum A D6 0,01 g; Acidum alpha-liponicum D6 0,01 g; Natrium diethyloxalaceticum D6 0,01 g; Acidum silicicum D6 1,0 g. Hydrophilic ointment (DAB 10) cont.:  emulsifying cetylsteryl alcohol, viscus paraffin, white Vaseline, purified water, ethanol.Preservative:  12,9% v/v ethyl alcohol.
Indications: This medicine is prepared in accordance with homeopathic principles and is proposed for use in arthrosis (in particular gonarthrosis); polyarthrosis, spondylarthrosis, scapulohumeral periarthritis.
Contraindications: This medication must not be administered to patients with hypersensitivity to  Arnica, to the genus Rhus of the Anacardiaceae family or to ingredients of the ointment base.
Warnings: A temporary aggravation of the existing symptoms is possible after taking a homeopathic preparation.
Interactions: None known.
Pregnancy and lactation: If you are pregnant or breast feeding your baby please consult your doctor, pharmacist or other health care professional for advice before taking this medicine.
Dosage and directions for use: Unless prescribed otherwise:  Apply to the affected areas in the morning and evening, e.g. rubbing in gently a 4-5 cm long ribbon of ointment at the area of the knee-joint.  Always tell your health care professional if you are taking any other medicine.  In the event of over dosage, consult your doctor or pharmacist.  If neither is available, contact the nearest poison control centre.
Side Effects and Special Precautions: In very rare cases, allergic skin reactions may occur.  Not all side effects reported for this medicine are included in this leaflet.  Should your general health worsen or if you experience untoward effects while taking this medicine, please consult your doctor, pharmacist or other health care professional for advice.
Registration number: U5685(Act 101/1965).
Disclaimer: This medicine has not been evaluated by the Medicines Control Council. This medicine is not intended to diagnose, treat, cure or prevent any disease.