Dermalac Cream 12%
Natural health product licensed in Canada
- Licence holder
- Sun Pharma Canada Inc.
- NPN or DIN-HM
- 02239903
- Status
- Active licence
- Licence date
- 6 August 2008
- Revision date
- Not provided
- Form
- Crème
- Route of administration
- Topique
- Application type
- DIN de transition
Oral dose analysis does not apply without an established exclusively oral route.
Composition
Medicinal composition not provided.
Non-medicinal ingredients
Propyl paraben, Eau purifiée, Glycérine, Huile minérale légère, Alcool cétylique, Acide lactique, Ammonia Solution, Strong NF, (p)-hydroxybenzoate de méthyle, Polyoxyethylene Stearates, propylèneglycol, Méthylcellulose, Laureth 4, Polyoxyl 40 Stearate, Silicate d'aluminium et de magnésium
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes | Not specified | Not specified | 2 Tous les jours |
Uses authorised in Canada
For moderate to severe dry skin such as ichthyosis
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 external use only. Do not use on abraded or inflamed skin. If irritation develops, discontinue use and consult your physician. Contact with the eyes should be avoided, if this happens rinse thoroughly with water. Keep this and all medication out of the reach of children.
Source
Official Health Canada record, licence 02239903
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.