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Jointeeze Devils Claw tablets – patient leaflet, side effects, dosage

Last updated: · Text from the MHRA, as of · About this document

Patient leaflet - Jointeeze Devils Claw tablets

1. WHAT THE PRODUCT IS AND WHAT IT IS USED FOR

This is a traditional herbal medicinal product containing Devil’s Claw root dry extract used for the relief of backache, rheumatic and muscular pain, and general aches and pains in the muscles and joints based on traditional use only.

2. BEFORE YOU TAKE THIS PRODUCT

This product is not suitable for patients under 18 years of age.

Do not take this product if:

  • you are allergic to Devil’s Claw (also known as Harpagophytum), or any of the other ingredients (see section 6 for more information).
  • you have, or have ever had either a stomach and/or a duodenal ulcer.

Take special care with this product:

  • If your condition is accompanied by swelling of the joint, redness or fever, consult your doctor.
  • You must consult a doctor or qualified healthcare practitioner if symptoms worsen or do not improve after 4 weeks.
  • If you have gallstones, consult a doctor before taking this product.
  • This product contains glucose. If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this product.
  • Do not exceed the recommended dose.

Taking other medicines.

Tell your doctor about any other medicines you are taking, including any bought without a prescription. Pregnancy and breast-feeding.

Do not take this product if you are pregnant or breastfeeding, because there is no evidence that it is safe to do so.

Driving and operating machines.

Devil’s Claw may make you feel dizzy and drowsy. If affected do not drive or operate machinery. Read all of this leaflet carefully because it contains important information for you.

This medicine is available without prescription. However, you still need to use this product carefully to get the best results from it.

Keep this leaflet. You may need to read it again.

Ask your doctor, pharmacist, or qualified healthcare practitioner if you need more information or advice.

You must consult a doctor or qualified healthcare practitioner if symptoms worsen or do not improve after 4 weeks.

If any side effect gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor.

In this leaflet:

Size: 160x256mm

New: Update: Y

Process + Spot 1 Foil Blocking

+ Spot 2 + Spot 3 + Spot 4

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Paper: --

Size: 160x256mm

Folded Size: 160x33mm

Colours: Special:

Additional Comments:

Saved: 13/10/22 By (Initials): JD

Certification

Mark

For a large print, braille or audio version of this leaflet please call 01772 686231

3. HOW TO TAKE THIS PRODUCT

For oral use only.

For adults and the elderly: swallow one tablet three times daily after food.

You must consult a doctor or qualified healthcare practitioner if symptoms worsen or do not improve after 4 weeks.

Do not take if you are under 18 years of age.

If you take too much of this product (overdose).

There are no reports of any adverse effects of overdosing, but if you have taken more than you should and feel unwell, talk to your doctor or qualified healthcare practitioner as soon as possible. If you forget to take this product.

Do not take a double dose to make up for a forgotten dose. Take the next dose when it becomes due. If you have any questions or are not sure how to take this product, consult your doctor or qualified healthcare practitioner.

4. POSSIBLE SIDE EFFECTS

Like all medicines, this product can cause side effects, although not everybody gets them. The frequency of side effects is not known.

Possible side effects include:

Digestive system:

  • Nausea, or feeling sick
  • Abdominal pain
  • Digestive upsets such as vomiting or diarrhoea

Other side effects:

  • Allergic reactions such as rash, itching and swelling of the face
  • Headaches
  • Dizziness

If you find these effects troublesome, stop using the product. Speak to your doctor or pharmacist if you are at all concerned, if a side effect becomes serious, or you notice an effect not mentioned in this leaflet. Reporting of side effects If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine.

5. HOW TO STORE THIS PRODUCT

Keep out of the reach and sight of children.

Do not store above 25°C.

Do not use this product after the expiry date which is stated on the base of the carton and the side of the bottle label after EXP. The expiry date refers to the last day of that month.

Do not use this product if you notice any discolouring or softening of the tablets, as this means they may have deteriorated.

Medicines should not be disposed of via wastewater or household waste. Ask you pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.

6. FURTHER INFORMATION

One film-coated tablet contains 300mg of extract (as dry extract) from Devil’s Claw root (Harpagophytum procumbens D.C. and/or H. zeyheri L. Decne radix), equivalent to 1050 – 1500mg Devil’ s Claw root. Extraction solvent: Ethanol 60%v/v.

Other ingredients:

Herbal extract – maltodextrin, silica colloidal anhydrous;

Tablet core – calcium hydrogen phosphate dihydrate, cellulose microcrystalline, crosscarmellose sodium, silica colloidal hydrated, magnesium stearate;

Coating – lecithin, croscarmellose sodium, glucose monohydrate, sodium citrate, dextrin. The product is available in packs of 30, 60, 90 and 120 tablets (not all sizes may be marketed). Registration number: THR 33336/0004

Traditional Herbal Registration Holder and Manufacturer:

Natures Aid Ltd, St Georges Park, Preston, Lancs PR4 2DQ

Tel: 01772 686231 Email: sales@naturesaid.co.uk

This leaflet was last revised on 10/2022.

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: THR333360004

Last revision stated in the text: October 2022 · MHRA data as of 13 October 2026

Found a mistake? Tell us on the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Facts about Jointeeze Devils Claw tablets

Pharmaceutical form Brown circular, biconvex tablets
Excipients Maltodextrin, Silica colloidal anhydrous, Calcium hydrogen phosphate dihydrate, Cellulose microcrystalline, Croscarmellose sodium, Silica colloidal hydrated, Magnesium stearate, Crosscarmellose sodium, Lecithin, Glucose monohydrate, Sodium citrate, Dextrin
Shelf life 3 years
Storage Do not store above 25°C. Store in original package.
Marketing authorisation THR 33336/0004 (first authorised 23 February 2011)
Marketing authorisation holder Natures Aid Ltd

Sources: the MHRA product information (products.mhra.gov.uk). Contains public sector information licensed under the Open Government Licence v3.0.