Wednesday, October 5, 2016

Balmosa Cream





1. Name Of The Medicinal Product



BALMOSA CREAM


2. Qualitative And Quantitative Composition



Active ingredients:



Menthol BP 2.0% w/w



Camphor BP 4.0% w/w



Methyl Salicylate Ph.Eur. 4.0% w/w



Capsicum Oleoresin BPC 0.035% w/w



3. Pharmaceutical Form



Cream for cutaneous use.



4. Clinical Particulars



4.1 Therapeutic Indications



Analgesic/rubefacient cream for the symptomatic relief of muscular rheumatism, fibrositis, lumbago, sciatica and unbroken chilblains.



4.2 Posology And Method Of Administration



Adults and the elderly:



Apply topically. Massage gently into the affected area as required. Wash hands immediately after use.



Children under 12 years:



Not generally recommended.



4.3 Contraindications



Hypersensitivity to aspirin, other non-steroidal anti-inflammatory drugs, or any of the ingredients listed.



4.4 Special Warnings And Precautions For Use



For external use only.



If skin sensitivity reactions occur, discontinue use. Do not apply to inflamed or broken skin. Avoid contact with the eye and mucous membranes. Do not apply to the nostrils of infants. Do not use with occlusive dressings.



After use avoid exposing the affected area to excessive sunlight.



4.5 Interaction With Other Medicinal Products And Other Forms Of Interaction



None stated.



4.6 Pregnancy And Lactation



With all salicylates there is animal evidence of teratogenicity. Use should be avoided during pregnancy and breast feeding.



4.7 Effects On Ability To Drive And Use Machines



None stated.



4.8 Undesirable Effects



Skin sensitivity reactions are possible although rare. Topical applications of large amounts of Balmosa Cream may result in systemic effects, including hypersensitivity and worsening of asthma.



4.9 Overdose



Overdosage is extremely unlikely from topical use.



5. Pharmacological Properties



5.1 Pharmacodynamic Properties



Capsicum oleoresin is a rubefacient. Camphor exhibits counter-irritant and weak local anaesthetic activity. Menthol and methyl salicylate impart analgesic properties to the formulation.



5.2 Pharmacokinetic Properties



Not applicable



5.3 Preclinical Safety Data



There are no preclinical data of relevance to the prescriber which are additional to that already included in other sections of the SPC.



6. Pharmaceutical Particulars



6.1 List Of Excipients



Methylcellulose



White soft paraffin



Emulsifying wax



Liquid paraffin



Lanolin (anhydrous)



Phenonip



Purified Water



6.2 Incompatibilities



None stated.



6.3 Shelf Life



3 years



6.4 Special Precautions For Storage



Do not store above 25oC.



6.5 Nature And Contents Of Container



Aluminium tube with a polyethylene cap containing 20g or 40g of the product.



6.6 Special Precautions For Disposal And Other Handling



None stated.



7. Marketing Authorisation Holder








Forest Laboratories UK Limited




Bourne Road




Bexley




Kent DA5 1NX



8. Marketing Authorisation Number(S)



PL 0108/5000R



9. Date Of First Authorisation/Renewal Of The Authorisation



18 March 1983 / 22 May 2003



10. Date Of Revision Of The Text



April 2003.



11. Legal Category


GSL




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