1. Name Of The Medicinal Product
Betadine Antiseptic Paint.
2. Qualitative And Quantitative Composition
Povidone Iodine USP 10% w/v.
3. Pharmaceutical Form
Cutaneous solution.
4. Clinical Particulars
4.1 Therapeutic Indications
As a general antiseptic paint in the prevention and treatment of infections.
4.2 Posology And Method Of Administration
For topical administration. Adults, children and the elderly: Apply Betadine Antiseptic Paint undiluted as necessary to the affected area and allow to dry. Rinse the brush thoroughly after use.
4.3 Contraindications
Hypersensitivity to iodine. History of abnormal thyroid function or goitre.
4.4 Special Warnings And Precautions For Use
If local irritation and hypersensitivity develop, then discontinue treatment.
4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction
None stated.
4.6 Pregnancy And Lactation
Use in pregnancy and lactation should be limited to minor lesions only. Although no adverse effects have been reported from limited use, caution should be recommended and therapeutic benefit must be balanced against possible effects of the absorption of iodine on foetal thyroid function and development.
4.7 Effects On Ability To Drive And Use Machines
None stated.
4.8 Undesirable Effects
Rarely, local irritation may occur.
4.9 Overdose
In the case of deliberate or accidental ingestion of large quantities, symptomatic and supportive treatment should be provided with special attention to electrolyte balance and thyroid function.
5. Pharmacological Properties
5.1 Pharmacodynamic Properties
Povidone iodine is a complex of iodine which shows all the broad-spectrum germicidal activity of elemental iodine. The germicidal activity is maintained in the presence of blood, pus, serum and necrotic tissue. It is effective in the treatment of infections caused by bacteria, fungi, yeasts and viruses (e.g. Herpes Virus Types I and II).
5.2 Pharmacokinetic Properties
None stated.
5.3 Preclinical Safety Data
None stated.
6. Pharmaceutical Particulars
6.1 List Of Excipients
Glycerol; nonoxynol 9; disodium hydrogen phosphate (anhydrous); citric acid monohydrate; industrial methylated spirit; sodium hydroxide (5% solution); purified water.
6.2 Incompatibilities
None stated.
6.3 Shelf Life
36 months unopened.
6.4 Special Precautions For Storage
Store below 25oC.
6.5 Nature And Contents Of Container
Glass bottle with a white polypropylene cap and applicator brush containing 8ml of product.
6.6 Special Precautions For Disposal And Other Handling
None stated.
7. Marketing Authorisation Holder
Seton Healthcare Group plc, Tubiton House, Oldham, OL1 3HS.
8. Marketing Authorisation Number(S)
PL 0223/0011.
9. Date Of First Authorisation/Renewal Of The Authorisation
28th April 1993 / 8th November 2003.
10. Date Of Revision Of The Text
November 2003.
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