Outgro
Natural health product licensed in Canada
- Licence holder
- Medtech Products, Inc.
- NPN or DIN-HM
- 02231569
- Status
- Active licence
- Licence date
- 28 March 2008
- Revision date
- 26 July 2012
- Form
- Liquide
- 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
Alcool, FD & C Rouge # 40, FD&C Blue #1, Jaune D & C No. 10, Poly(éthylène glycol)
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes | Not specified | Not specified | minimum: 3 Tous les jours ; maximum: 4 Tous les jours |
| Enfants | minimum: 2 years | Not specified | minimum: 3 Tous les jours ; maximum: 4 Tous les jours |
Uses authorised in Canada
A topical local anesthetic for the temporary relief of pain associated with minor skin irritations.
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 02231569
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.
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 2012. Photograph the packaging to check whether it has changed.
Has the product changed? Photograph the packaging.