CompoAtlas

Nexultra UV

Natural health product licensed in Canada

Licence holder
UNIVERSKIN AMERICAS INC.
NPN or DIN-HM
80111384
Status
Active licence
Licence date
15 July 2021
Revision date
Not provided
Form
Poudre
Route of administration
Topique
Application type
Officinale

Oral dose analysis does not apply without an established exclusively oral route.

Composition

Medicinal ingredient and sourcePer dosage unit, according to the source
Dioxyde de titane

Source : Dioxyde de titane

22 %

Non-medicinal ingredients

Polymère croisé de diméthicone/vinyl diméthicone, C.I. 77492, Polymère croisé de vinyl diméthicone/méthicone silsesquioxane, Acétyle hexapeptide-1, Phospholipides, Acide stéarique, Dextrane, Talc, Diméthicone, Chlorphénésine, Glycérine, Salicylate de butyloctyle, Hydroxyéthylcellulose, Silicate de magnésium et d'aluminium, Alumine, Mica

PopulationAgeQuantity per servingFrequency
Adultesminimum: 19 yearsNot specifiedNot specified

Uses authorised in Canada

Text supplied in English because no French text is available.

Broad spectrum (Sun Protection Factor 50+ / SPF 50+). Sun Protection Factor 50+ / SPF 50+. UVA/UVB protection.

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 80111384

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.

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