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Methyl salicylate with camphor, capsicum oleoresin and menthol

Presentation

Cream containing 2% menthol, 4% camphor, 4% methyl salicylate and 0.035% oleoresin capsicum.
Cream containing 2.54% menthol, 1.43% camphor, 0.42% methyl salicylate and 0.005% oleoresin capsicum

Drugs List

  • BALMOSA cream
  • methyl salicylate with camphor oleoresin capsicum and menthol cream
  • RADIAN B rub
  • Therapeutic Indications

    Uses

    For the symptomatic relief of muscular and rheumatic aches and pains, including muscular stiffness, bruising, sprains, fibrositis, lumbago, sciatica and unbroken chilblains.

    Not all brands are licensed for all indications.

    Dosage

    Adults

    Massage gently into the affected area

    Elderly

    Massage gently into the affected area

    Children

    Under 12 years of age

    Not recommended.

    (Some brands may not be recommended for children under 6 years.)

    Adolescents

    Massage gently into the affected area

    Administration

    For topical administration.

    Wash hands immediately after use.

    For muscular strains and stiffness it is best used after a hot bath.

    Precautions and Warnings

    If skin sensitivity reactions occur, discontinue use.

    Do not apply to inflamed or broken skin.

    Avoid contact with the eyes and mucous membranes.

    Do not use with occlusive dressings.

    Advise patient to avoid exposing the treated area to direct sunlight.

    Not all brands are licensed for all age groups.

    Not all brands are licensed for all indications.

    Pregnancy - see 'Pregnancy' section

    Lactation - see 'Lactation' section

    Pregnancy and Lactation

    Pregnancy

    Use of this product should be avoided during pregnancy unless there is no safer alternative.

    With all salicylates there is animal evidence of teratogenicity.

    The use of all medication in pregnancy should be avoided whenever possible; particularly in the first trimester. Non-drug treatments should also be considered. When essential, a medication with the best safety record over time should be chosen, employing the lowest effective dose for the shortest possible time. Polypharmacy should be avoided. Teratogens taken in the pre-embryonic period, often quoted as lasting until 14-17 days post-conception, are believed to have an all-or-nothing effect. Where drugs have a short half-life, and when the date of conception is certain, this may allow women to be reassured where drug exposure has occurred within this time frame. Further advice may be available from the UK National Teratology Information Service (NTIS) and through ToxBase, available via password on the internet ( www.toxbase.org ) or if this is unavailable at the backup site ( www.toxbasebackup.org ).

    Licensed in pregnancy? - No

    Recommended for use in pregnancy? - No

    Animal data - shows evidence of teratogenicity

    Lactation

    Some brands are considered by the manufacturer to be safe for use during breast-feeding - consult product literature.

    Neonates, infants born prematurely, those with low birth weight, those with an unstable gastrointestinal function or who have serious illnesses may require special consideration. For any infant, if a drug is prescribed to the nursing mother, it should be at the lowest practical dose and for the shortest time. When drug administration is unavoidable and breastfeeding is to continue, minimisation of exposure of the infant to the drug may sometimes be achieved by timing the maternal doses to just after a feeding episode. Infants exposed to drugs via breast milk should be monitored for unusual signs or symptoms. Interactions between the drug received by the infant from the mother's milk and medication prescribed for the infant should also be considered, for example, when the drug given to the infant may prevent metabolism of the drug received via breast milk.
    Specialist advice is available from the UK Drugs in Lactation Advisory Service at https://www.midlandsmedicines.nhs.uk/content.asp?section=6&subsection=17&pageIdx=1

    Side Effects

    Hypersensitivity reactions
    Contact dermatitis
    Eczema
    Urticaria
    Headache
    Flushing

    Topical application of large amounts may result in systemic effects, including hypersensitivity reactions and worsening of asthma.

    Overdosage

    It is strongly recommended that the UK National Poisons Information Service be consulted on cases of suspected or actual overdose where there is doubt over the degree of risk or about appropriate management.

    The following number will direct the caller to the relevant local centre (0844) 892 0111

    Information may be obtained if you have access to ToxBase the primary clinical toxicology database of the National Poisons Information Service. This is available via password on the internet ( www.toxbase.org ) or if this is unavailable at the backup site ( www.toxbasebackup.org ).

    Shelf Life and Storage

    Do not store above 25 degrees C

    Reference Sources

    Summary of Product Characteristics: Balmosa Cream. Forest Laboratories UK Limited. Revised April 2003

    Summary of Product Characteristics: Radian B Muscle Rub. Thornton & Ross Ltd. Revised December 2003

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    Medscape UK | Univadis prescription drug monographs & interactions are based on FDB Multilex Content

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    FDB Disclaimer : FDB Multilex is intended for the use of healthcare professionals and is provided on the basis that the healthcare professionals will retain FULL and SOLE responsibility for deciding what treatment to prescribe or dispense for any particular patient or circumstance.