1. Name Of The Medicinal Product
Sting Relief
2. Qualitative And Quantitative Composition
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3. Pharmaceutical Form
Cream
4. Clinical Particulars
4.1 Therapeutic Indications
Treatment of insect bites and stings, including bee and wasp stings and the bites of mosquitoes, gnats and other insects.
For topical administration to the skin.
4.2 Posology And Method Of Administration
Adults, children and elderly
Massage a little of the cream gently into the affected area.
Repeat the application every two or three hours if necessary.
4.3 Contraindications
Hypersensitivity to any of the ingredients.
4.4 Special Warnings And Precautions For Use
For external use only.
Keep all medicines out of the reach of children.
4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction
No clinically significant interactions known.
4.6 Pregnancy And Lactation
The safety of Sting Relief during pregnancy and lactation has not been established, but use of the product is not considered to be contraindicated during these periods.
4.7 Effects On Ability To Drive And Use Machines
No adverse effects known.
4.8 Undesirable Effects
Occasional hypersensitivity and irritant reactions.
4.9 Overdose
Over application to the skin may cause an irritant reaction. The use of Sting Relief should be immediately discontinued and symptomatic treatment provided.
In cases of oral ingestion, there may be burning in the gastrointestinal tract, nausea and vomiting. Treatment should be symptomatic and supportive. Only in severe cases would active therapy, including gastric aspiration and lavage, be necessary.
5. Pharmacological Properties
5.1 Pharmacodynamic Properties
Zinc oxide has mild astringent and soothing properties as well as being protective.
Benzyl alcohol is a weak local anaesthetic with disinfectant properties.
Chloroxylenol is an antiseptic with particular activity against gram positive organisms.
Eucalyptus oil has an irritant and rubefacient action which produces mild local anaesthesia.
5.2 Pharmacokinetic Properties
No data available
5.3 Preclinical Safety Data
There are no preclinical data of relevance to the prescriber which are additional to that already included.
6. Pharmaceutical Particulars
6.1 List Of Excipients
Japan wax
Liquid paraffin
Polawax
Purified water
6.2 Incompatibilities
None stated.
6.3 Shelf Life
36 months.
6.4 Special Precautions For Storage
None.
6.5 Nature And Contents Of Container
Collapsible aluminium tube, internally lacquered with an epoxy resin, with polyethylene caps or a collapsible aluminium tube internally lacquered with an epoxy resin with a membrane seal and a polyethylene or polypropylene cap with a piercer device.
Pack sizes: 14gm or 15gm.
The tube will be packed in a carton.
6.6 Special Precautions For Disposal And Other Handling
None stated.
7. Marketing Authorisation Holder
The Boots Company PLC
1 Thane Road West
Nottingham NG2 3AA
8. Marketing Authorisation Number(S)
PL 00014/0377
9. Date Of First Authorisation/Renewal Of The Authorisation
First Authorisation: 22 May 1989
Last Renewal: 15 September 1999
10. Date Of Revision Of The Text
May 2004
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