I Arthritis Combin
HOMEOFORCE TISSUE SALTS I ARTHRITIS COMBIN is a combination of the following Tissue Salts: Ferrum phosphoricum, Kali sulphuricum, Magnesia phosphorica, Natrum phosphoricum and Natrum sulphuricum.
It is indicated for Arthritis, Sciatica & Backache
Dosage:
- adults: 1 tablet
- children: Half a tablet
- infants: A quarter tablet, crushed and dissolved in water.
- general: Dissolve tablet(s) under the tongue 3 times daily.
- acute: Dissolve tablet(s) under the tongue every half an hour (up to 12 times a day) or until improvement of symptoms, then resume general dosing.
Ingredients:
- Calcium fluoride (Calcarea fluorica)
- Calcium phosphate (Calcarea phosphorica)
- Calcium sulphate (Calcarea sulphurica)
- Iron phosphate (Ferrum phosphoricum)
- Potassium sulphate (Kali sulphuricum)
- Magnesium phosphate (Magnesia phosphorica)
- Sodium phosphate (Natrum phosphoricum)
- Inactive ingredients: Lactose and magnesium stearate.
- Contains sugar: Lactose 0.24 g/tablet.
- Suitable for vegetarians.
Contraindications:
- Do not use HOMEOFORCE TISSUE SALTS I ARTHRITIS COMBIN if you are hypersensitive (allergic) to any of the ingredients.
Warnings & Special Precautions
If you are on any medication or suffering from any medical condition, it is advisable to seek medical advice before starting any new medicine, supplement or remedy.
Do not exceed recommended dosage(s) unless on the advice of a healthcare practitioner. Contains lactose. Patients with the rare hereditary conditions of galactose intolerance e.g. galactosaemia, Lapp lactase deficiency or glucose-galactose malabsorption should not take HOMEOFORCE TISSUE SALTS I ARTHRITIS COMBIN.
Contains lactose which may have an effect on the glycaemic control of patients with diabetes mellitus. This unregistered medicine has not been evaluated by SAHPRA for its quality, safety or intended use. Tissue Salts are safe in pregnancy and lactation; however, you should always consult with your healthcare provider.
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For full prescribing information, refer to the Professional Information approved by the medicines regulatory authority.