CompoAtlas

Itch FX

Natural health product licensed in Canada

Licence holder
JRC Pharmaceuticals
NPN or DIN-HM
80085832
Status
Active licence
Licence date
4 June 2018
Revision date
Not provided
Form
Solution
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
(11bêta)-11,17,21-trihydroxy-prégn-4-ène-3,20-dione

Source : Hydrocortisone

0.5 Pour cent

Non-medicinal ingredients

Propylène glycol, Eau

PopulationAgeQuantity per servingFrequency
Adultes et enfantsminimum: 2 yearsNot specifiedNot specified

Uses authorised in Canada

For temporary relief of minor skin irritations, rashes, itching and redness due to eczema, insect bites, poison ivy, poison oak, poison sumac, contact dermatitis, seborrheic dermatitis, psoriasis.

A use authorised in Canada is not an authorised health claim in the European Union. See the health claims register.

Warnings in Canada

Source

Official Health Canada record, licence 80085832

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.

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