RADIUM SALIL CREAM 60 G
Description
ACTION AND MECHANISM
Analgesic, anti-inflammatory and rubefacient.
SPECIAL WARNINGS
- If symptoms persist for more than 7 days or irritation or worsening occurs, the patient's clinical situation should be evaluated.
PATIENT ADVICE
- Avoid contact with the eyes and mucous membranes.- Do not use with occlusive dressings or apply simultaneously to the same area as other topical preparations.- Do not use for prolonged periods or over large areas.- Use only on intact skin; do not use on open wounds, mucous membranes, or eczematous skin.- Do not expose the treated area to the sun.- Wash your hands after each application.
CONTRAINDICATIONS
[SALICYLATE ALLERGY] or [NSAID ALLERGY] or to any of the components of this medicine.- Although local administration minimizes the risks derived from its systemic use, topical application, in large areas of the skin, in open wounds, mucous membranes or eczematous skin, for a prolonged period and with the use of occlusive dressings, can cause systemic effects, so it is worth remembering that its use is not recommended in patients who have presented allergic reactions (rhinitis, asthma, pruritus, angioedema, urticaria, shock or others), caused by acetylsalicylic acid or other NSAIDs due to the possibility of cross-hypersensitivity.
PREGNANCY
Safety has not been established during pregnancy. Use in these circumstances should be based on medical judgment, assessing the benefit/risk, as the components can be absorbed systemically through the skin, causing systemic effects.
INDICATIONS
- Symptomatic local relief of painful or inflammatory conditions of traumatic or degenerative origin in the joints, tendons, ligaments and muscles ([ARTHRITIS], periarthritis, [CAPSULITIS], arthrosinovitis, [TENDINITIS], [TENOSYNOVITIS], [BURSITIS], distortions, [TORTICOLLIS], [LOW BACK PAIN], [CONTUSION], [SPRAIN], [CONTRACTURE], [DISLOCATION]).
INTERACTIONS
They have not been described for cutaneous use, since very low systemic concentrations of the drug are achieved, but it will be assessed whether they should be used in conjunction with other topical analgesics.
LACTATION
Safety during breastfeeding has not been established. Although systemic absorption is very low when applied cutaneously, the preparation should not be used during breastfeeding unless medically necessary, as the components can cross the placental barrier.
CHILDREN
Not recommended for use in children under 12 years of age.
RULES FOR CORRECT ADMINISTRATION
- Apply a thin layer of the product to the affected area with a light massage to facilitate penetration. - Wash your hands after each application.
POSOLOGY
DOSAGE:- For external use only.- Adults and children over 12 years: apply 2 to 4 times a day.- Do not apply for more than 7 consecutive days without consulting a doctor.
PRECAUTIONS RELATED TO EXCIPIENTS
- Because it contains cetyl alcohol, it can cause local skin reactions, such as contact dermatitis.
ADVERSE REACTIONS
- [ERYTHEMA], [PRURITUS], sensation of [SKIN IRRITATION] at the application site and local allergic sensitization, effects that subside upon discontinuation of application.
OVERDOSE
- Symptoms: Prolonged application and/or application to large areas may cause salicylate poisoning (dizziness, vomiting, ringing in the ears, blurred vision, drowsiness). In this case, you should discontinue the medication and seek medical advice. - Treatment: In case of accidental ingestion, induce vomiting and/or gastric lavage or symptomatic treatment as determined by a doctor.
COMPOSITION
CAMPHOR: 20 MILLIGRAMS
METHYL NICOTINATE: 10 MILLIGRAMS
METHYL SALICYLATE: 100 MILLIGRAMS
SALICYLIC ACID: 20 MILLIGRAMS
MENTHOL: 50 MILLIGRAMS
PROPYLENE GLYCOL (EXCIPIENT): 0
CETYL ALCOHOL (EXCIPIENT): 0
Features
| Product code | 505730 |
| Category | Joints and Bone System, Bone and Muscle Diseases |
| Volume | 60 g |
| Delivery from | Spain |
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