BP Drops
BP Drops, licence 80038597: active licence in Health Canada data. The French and European references below do not constitute authorisation for sale in France or an assessment of safety or efficacy.
Licensed Natural Health Products Database (LNHPD), Health Canada: licensed products, ingredients, doses, uses and risks, retrieved 27 October 2026.
Contains information licensed under the Open Government Licence – Canada (Health Canada, LNHPD)
Licence du gouvernement ouvert – Canada 2.0 (OGL-Canada 2.0)
Natural health product licensed in Canada
- Other names
- Diuretic Drops, Edema Drops, K & BP Drops, Kidney & BP Drops, Kidney Drops, Kidney Support Drops
- Licence holder
- Strauss Naturals Limited
- NPN or DIN-HM
- 80038597
- Status
- Active licence
- Licence date
- 9 January 2013
- Revision date
- 17 April 2024
- Form
- Teinture
- Route of administration
- Orale
- Application type
- Non traditionnelle
If this product were sold in France
- Conditions légales
Salix alba L.: L'étiquetage doit comporter un avertissement déconseillant l'emploi aux personnes souffrant d'allergie aux dérivés salicylés.
arrêté du 24 juin 2014, annexe I. French orders of 9 May 2006 (nutrients), 24 June 2014 (plants) and 26 September 2016 (other substances), consolidated LEGI collection, retrieved 23 October 2026.
- Conditions légales
Urtica dioica L.: L'étiquetage des compléments alimentaires contenant les parties souterraines de cette plante doit comporter une mention recommandant de prendre conseil auprès d'un professionnel de santé ("Demander l'avis de votre médecin et /ou pharmacien").
arrêté du 24 juin 2014, annexe I. French orders of 9 May 2006 (nutrients), 24 June 2014 (plants) and 26 September 2016 (other substances), consolidated LEGI collection, retrieved 23 October 2026.
- Conditions légales
Leonurus cardiaca L.: L'étiquetage doit comporter un avertissement déconseillant l'emploi chez les femmes enceintes
arrêté du 24 juin 2014, annexe I. French orders of 9 May 2006 (nutrients), 24 June 2014 (plants) and 26 September 2016 (other substances), consolidated LEGI collection, retrieved 23 October 2026.
- Conditions légales
Juniperus communis L.: L'étiquetage doit comporter un avertissement recommandant de ne pas utiliser en cas d'insuffisance rénale et un avertissement recommandant de ne pas utiliser de manière prolongée (maximum 6 semaines)
arrêté du 24 juin 2014, annexe I. French orders of 9 May 2006 (nutrients), 24 June 2014 (plants) and 26 September 2016 (other substances), consolidated LEGI collection, retrieved 23 October 2026.
A daily quantity is calculated only for an explicit adult oral dosage, stated per day and in a solid unit matching the product form. Ambiguous units, liquids, powders and paediatric doses are not extrapolated. A quantity not calculated is not compared with dose limits. This analysis does not constitute authorisation for sale in France or an assessment of safety or efficacy.
Composition
| Medicinal ingredient and source | Per dosage unit, according to the source | Maximum per day, adult |
|---|---|---|
| Althaea officinalis Source : Racine Extraction ratio : 1:53.4299 Dry plant equivalent : 12.9 mg | 690.0 µL/mL | Not calculated |
| Salix alba Source : Écorce Extraction ratio : 1:2 Dry plant equivalent : .4 mg | 0.8 mL | Not calculated |
| Viscum album Source : Feuille Extraction ratio : 1:2 Dry plant equivalent : 5.6 mg | 11.1 µL/mL | Not calculated |
| Urtica dioica Source : Feuille Extraction ratio : 1:124.424 Dry plant equivalent : 5.6 mg | 690.0 µL/mL | Not calculated |
| Leonurus cardiaca Source : Parties aériennes Extraction ratio : 1:2 Dry plant equivalent : 1 mg | 1.9 µL/mL | Not calculated |
| Capsicum annuum Source : Fruit Extraction ratio : 1:2 Dry plant equivalent : .7 mg | 1.5 µL/mL | Not calculated |
| Juniperus communis Source : Fruit Extraction ratio : 1:12.615 Dry plant equivalent : 54.7 mg | 690.0 µL/mL | Not calculated |
| Crataegus laevigata Source : Fruit Extraction ratio : 1:2 Dry plant equivalent : 11.1 mg | 22.2 µL/mL | Not calculated |
| Allium sativum Source : Bulbe Extraction ratio : 1:2 Dry plant equivalent : 135 mg | 270.0 µL/mL | Not calculated |
Non-medicinal ingredients
Éthanol, Eau
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes | Not specified | 3.0 mL | minimum: 2.0 Tous les jours ; maximum: 3.0 Tous les jours |
Uses authorised in Canada
Text supplied in English because no French text is available.
Juniper, goldenrod, uva-ursi, parsley, gravel, horesetail, and nettle are traditionally used in Herbal Medicine as diuretics to help relieve symptoms of temporary water retention, such as edema.
A use authorised in Canada is not an authorised health claim in the European Union. See the health claims register.
Warnings in Canada
No French warning text available in the imported data.
Warnings are available in English on the official record.
Source
Official Health Canada record, licence 80038597
The formula sold in Europe under the same name may differ. This information does not replace advice from a doctor or pharmacist.
List in the official revision dated (register: Licensed Natural Health Products Database (LNHPD), Health Canada: licensed products, ingredients, doses, uses and risks).
List recorded in 2024. Photograph the packaging to check whether it has changed.
Has the product changed? Photograph the packaging.