Deep Relief Gel, an anti-inflammatory Triple Action gel contains levomenthol and the painkiller ibuprofen. The gel is intended for direct application to areas of pain and inflammation and provides fast-acting, targeted pain relief.
Effective for the relief of rheumatic pain, muscular aches and swellings, and sports injuries.
Ibuprofen penetrates the skin to provide effective targeted pain and inflammation relief helping to reduce swelling. Levomenthol cools and soothes to help provide pain relief to the inflamed area.
For adults, the elderly, and children over 12 years. Please follow the instructions on the enclosed leaflet.
Use this medicine only on your skin.
Apply 1-4cm of gel as a thin layer up to 3 times per day.
Do not use more often than every 4 hours.
If symptoms persist consult your doctor or pharmacist.
Please read the enclosed leaflet carefully before use. Do not use if you are allergic to ibuprofen, menthol, any of the ingredients, aspirin or any other painkillers. Do not use if you are more than 6 months pregnant or if you are breastfeeding. Consult your doctor before use if you are taking aspirin, any painkillers or if you are pregnant. Do not use after the expiry date. Store below 25˚C. Keep all medicines out of the sight and reach of children.
Read the enclosed leaflet before use.
Active Ingredients: Ibuprofen 5.0% w/w, Levomenthol 3.0% w/w Also contains: Carbomer, Propylene Glycol, Di-isopropanolamine, Ethanol, Purified Water
Skin disorders are most frequently reported: Application site reactions such as, rashes, pruritus and urticaria, drying, reddening, burning sensation, contact dermatitis.
Other systemic undesirable effects of NSAIDs depend on the quantity of gel applied, the treated area, the integrity of the skin, the duration of treatment, the use of occlusive dressings: although extremely uncommon when administered topically side effects such as abdominal pain, dyspepsia and renal impairment are possible.
Hypersensitivity reactions have been reported following treatment with ibuprofen. These may consist of:
(a) Non-specific allergic reactions and anaphylaxis.
(b) Respiratory tract reactivity comprising of asthma, aggravated asthma,
dyspnoea and bronchospasm may be precipitated in patients suffering from
or with a previous history of bronchial asthma or allergic disease (see
(c) Assorted skin disorders, including rashes of various types, pruritus,
urticaria, purpura, angioedema and, less commonly, bullous dermatoses
(including epidermal necrolysis and erythema multiforme).
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the national reporting system:
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Proven treatment for muscular aches and pains