Post Procedure Recovery System
Natural health product licensed in Canada
- Licence holder
- ZO Skin Health Inc.
- NPN or DIN-HM
- 80072555
- Status
- Inactive licence
- Licence date
- 15 September 2016
- Revision date
- 13 October 2016
- Form
- Kit
- Route of administration
- Topique
- Application type
- Non traditionnelle
Oral dose analysis does not apply without an established exclusively oral route.
Composition
| Medicinal ingredient and source | Per dosage unit, according to the source |
|---|---|
| Acide sulfurique, sel d'aluminum (3:2), tétradécahydraté Source : Sulfate d'aluminium tétradécahydraté | 2,850 mg |
| Avena sativa Source : Avena sativa - Graine | 1 % |
| Acide acétique, sel de calcium, monohydrate Source : Acétate de calcium monohydraté | 2,016 mg |
Non-medicinal ingredients
palmitate de rétinyle, Alcool isopropylique, bêta-glucane, Chlorure de benzalkonium, Glycérine, Palmitate d'isopropyle, Glycyrrhizate de dipotassium, Chlorure de sodium, pentylene glycol, Butylène glycol, Chitosane, Eau, Cyclopentasiloxane, alcool benzylique, Benzyl ether, Beurre de Butyrospermum Parkii (Karité), Protéine du grain d'Avena Sativa (avoine), Sorbate de potassium, Protéine de lactosérum, Myristoyl Pentapeptide-11, Pétrolatum, Tétrapeptide-21, Acide ascorbique, Méthacrylate de poly (méthyle), Dextrine, Alcool, 1,2-Hexanediol, Acétate de d-alpha tocophéryle, Distearyldimonium Chloride, Alcool cétylique, Protéine de Glycine Soja (Fève soja)
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes | Not specified | Not specified | Not specified |
Uses authorised in Canada
Text supplied in English because no French text is available.
Product #1 - REVITATROL: Temporarily protects and helps relieve minor skin irritation and itching due to rashes, eczema, poison ivy, poison oak or poison sumac, and insect bites. Product #2 - SURFATROL: Astringent solution (after dissolution of the powder) for the temporary relief of minor skin irritations and rashes.
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 80072555
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 2016. Photograph the packaging to check whether it has changed. Photograph the packaging