Venloxin LD Oral Spray
Natural health product licensed in Canada
- Other names
- VENLOXIN MD Oral Spray (140)
- Licence holder
- CobraMed Pharmaceuticals Limited
- NPN or DIN-HM
- 80031450
- Status
- Active licence
- Licence date
- 16 April 2012
- Revision date
- Not provided
- Form
- Solution
- Route of administration
- Sublinguale
- Application type
- Homéopathique
Oral dose analysis does not apply without an established exclusively oral route.
Composition
Medicinal composition not provided.
Non-medicinal ingredients
Phosphate de sodium, xylitol, Benzoate de sodium, Natural Citrus Flavour, Eau purifiée
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes | Not specified | 2 Pulvérisateur | 4 days |
Uses authorised in Canada
Text supplied in English because no French text is available.
Homeopathic Remedy for the temporary relief of pain including migraine, back pain, neck aches, shoulder pain, neuralgia.
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 80031450
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)
The formula sold in Europe under the same name may differ. This information does not replace advice from a doctor or pharmacist.
The evidence date of this ingredient list is unknown.
Has the product changed? Photograph the packaging.