Ultra Thin Medicated Corn Removers
Natural health product licensed in Canada
- Other names
- Medicated Callus Removers
- Licence holder
- Aetna Felt Corporation
- NPN or DIN-HM
- 80016092
- Status
- Inactive licence
- Licence date
- 23 February 2010
- Revision date
- Not provided
- Form
- Plâtre
- Route of administration
- Topique
- Application type
- Officinale
Oral dose analysis does not apply without an established exclusively oral route.
Composition
Medicinal composition not provided.
Non-medicinal ingredients
Dioxyde de silicium, Talc, Toluene, Rubber, Pétrole, Brown Dye, antioxidant
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Sous-population S/O | Not specified | 1 pansement adhésif | Not specified |
Uses authorised in Canada
Text supplied in English because no French text is available.
For the removal of corns and calluses.
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.
Source
Official Health Canada record, licence 80016092
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.