CompoAtlas

Hydrocortisone Cream 0.5%

Natural health product licensed in Canada

Licence holder
CRLS
NPN or DIN-HM
80039534
Status
Inactive licence
Licence date
5 February 2013
Revision date
Not provided
Form
Crème
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 %

Non-medicinal ingredients

Huile minérale, Propylène glycol, Eau purifiée, PEG-20 cétyl éther, Hydroxyde de sodium, Phosphate de sodium, monobasique, Pétrolatum, Acide phosphorique, Chlorocrésol

PopulationAgeQuantity per servingFrequency
Adultes et enfantsNot specified1 Crèmeminimum: 2 days ; maximum: 4 days

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, seborrheic dermatitis, psoriasis, contact dermatitis caused by soaps, detergents, cosmetics and/or jewellery.

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 80039534

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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