Country: United Kingdom
Language: English
Source: MHRA (Medicines & Healthcare Products Regulatory Agency)
Racemic camphor; Salicylic acid
Scholl's Wellness Company Ltd
Racemic camphor; Salicylic acid
31.1mg/1gram ; 125mg/1gram
Cutaneous solution
Cutaneous
No Controlled Drug Status
Valid as a prescribable product
BNF: 13070000; GTIN: 5052197021288
OBJECT 1 SCHOLL SEAL AND HEAL VERRUCA REMOVAL GEL Summary of Product Characteristics Updated 24-Jan-2017 | Reckitt Benckiser Healthcare (UK) Ltd • 1. Name of the medicinal product • 2. Qualitative and quantitative composition • 3. Pharmaceutical form • 4. Clinical particulars • 4.1 Therapeutic indications • 4.2 Posology and method of administration • 4.3 Contraindications • 4.4 Special warnings and precautions for use • 4.5 Interaction with other medicinal products and other forms of interaction • 4.6 Fertility, pregnancy and lactation • 4.7 Effects on ability to drive and use machines • 4.8 Undesirable effects • 4.9 Overdose • 5. Pharmacological properties • 5.1 Pharmacodynamic properties • 5.2 Pharmacokinetic properties • 5.3 Preclinical safety data • 6. Pharmaceutical particulars • 6.1 List of excipients • 6.2 Incompatibilities • 6.3 Shelf life • 6.4 Special precautions for storage • 6.5 Nature and contents of container • 6.6 Special precautions for disposal and other handling • 7. Marketing authorisation holder • 8. Marketing authorisation number(s) • 9. Date of first authorisation/renewal of the authorisation • 10. Date of revision of the text 1. Name of the medicinal product Scholl Corn and Callous Removal Liquid Scholl Medicated Corn and Callous Removal Liquid Seal and Heal Verruca Removal Gel 2. Qualitative and quantitative composition INGREDIENT % W/W Salicylic Acid EP 12.50 Camphor BP 3.11 For a full list of excipients, see section 6.1. 3. Pharmaceutical form Topical solution 4. Clinical particulars 4.1 Therapeutic indications For the treatment of corns, calluses, common warts and plantar warts (verrucas). 4.2 Posology and method of administration POSOLOGY Treatment may be continued for up to twelve weeks except on medical advice. Adults: Apply directly to the callus, corn, verruca or wart twice a day. Paediatric Population Children over 12 years: As above for adults. Children aged under 12 years of age: Not recommended for children under twelve. M Read the complete document