Pediavit Jr. Complete
Natural health product licensed in Canada
- Licence holder
- Euro-Pharm International Canada Inc.
- NPN or DIN-HM
- 80001818
- Status
- Inactive licence
- Licence date
- 13 June 2006
- Revision date
- Not provided
- Form
- Comprimé, à croquer
- Route of administration
- Orale
- Application type
- Officinale
If this product were sold in France
No point flagged by the rules we apply.
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 |
|---|---|---|
| Niacine | 15 mg | Not calculated |
| Vitamine D3 Potency : 400 UI | 0.01 mg | Not calculated |
| Thiamine | 1.5 mg | Not calculated |
Non-medicinal ingredients
Dioxyde de silicium colloïdal, Bubblegum flavour (artificial), Stéarate de magnésium, Dextrose, Saveur de raisin artificielle, Acide stéarique, Acide citrique, FD & C Jaune no. 6, Cyclamate de sodium, mannitol, Erythrosine, Sorbitol, FD&C Blue No.2, Saveur d'orange
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Enfants | minimum: 4 years ; maximum: 12 years | 1 Comprimé | Not specified |
Uses authorised in Canada
Vitamin and Mineral Supplement
A use authorised in Canada is not an authorised health claim in the European Union. See the health claims register.
Warnings in Canada
- Précautions et mises en garde
For therapeutic use only. Keep out of reach of children. Consult a physician prior to use if you have impaired liver function. Discontinue use if you experience a prolonged flushing, burning, tingling or itching sensation on the face, arms or chest. If this medication is used in an area where the water has a fluoride content in excess of 0.7 parts of fluoride per million parts of water, or is artificially fluoridated, mottling of teeth enamel may result. Consult a physician prior to use if you are taking tetracyclines. Consult a physician prior to use if you are taking levodopa. Avoid using two(2) hours prior to or until four (4) hours after taking other medications.
- Contre-indications
Do not use in the presence of a copper storage or metabolism disorder, such as Wilson's disease or if Leber's disease is present.
Source
Official Health Canada record, licence 80001818
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.