For practitioner dispensing and professionally guided use.
Always read the label and follow the directions for use.
Do not use if you have an active stomach or duodenal ulcer.
Consult your healthcare practitioner before use if you have a history of peptic ulceration, significant reflux or persistent gastrointestinal irritation.
Consult your doctor before use if you have gallstones or another gallbladder or bile-duct condition.
Do not use during pregnancy or breastfeeding unless specifically prescribed after professional assessment.
Not recommended for children or adolescents under 18 years unless specifically prescribed by an appropriately qualified healthcare practitioner.
Consult your healthcare practitioner before use if you take prescription medicines or have an existing medical condition.
Possible adverse effects include diarrhoea, nausea, vomiting, abdominal discomfort, headache, dizziness or an allergic reaction.
Stop use and seek urgent medical attention if facial swelling, breathing difficulty or another serious allergic reaction occurs.
Joint pain accompanied by marked swelling, redness or fever requires medical assessment.
Consult a healthcare professional if joint symptoms worsen or persist for more than four weeks.
Consult a healthcare professional if digestive symptoms worsen or persist for more than two weeks.
Do not use this product as a substitute for medical assessment or prescribed management of arthritis, injury or persistent pain.
Discontinue use at least seven days before general anaesthesia unless otherwise directed by your healthcare professional.
Contains ethanol.
Keep out of reach of children.
The EMA monograph contraindicates Devil’s Claw in active gastric or duodenal ulcer, advises medical review for gallstones, does not recommend use during pregnancy or breastfeeding because safety has not been established, and records gastrointestinal symptoms, headache, vertigo and hypersensitivity reactions as possible adverse effects.