First On Anti-Itch
Natural health product licensed in Canada
- Licence holder
- Arvidis, Inc.
- NPN or DIN-HM
- 80003628
- Status
- Active licence
- Licence date
- 21 June 2007
- Revision date
- Not provided
- Form
- Bâtonnet
- Route of administration
- Topique
- Application type
- Officinale
Oral dose analysis does not apply without an established exclusively oral route.
Composition
Medicinal composition not provided.
Non-medicinal ingredients
Lactate de menthyle, Stéarate de Sodium, Eau, Steareth 21, triéthanolamine, EDTA de tétrasodium, diazolidinyl urée, propylèneglycol, Butylcarbamate d'iodopropynyle, Alcool éthylique
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Enfants | minimum: 2 years | Not specified | minimum: 2 Tous les jours ; maximum: 4 Tous les jours |
| Adultes | Not specified | Not specified | minimum: 2 Tous les jours ; maximum: 4 Tous les jours |
| Enfants | maximum: 2 years | Not specified | Not specified |
Uses authorised in Canada
Temporary relief of itching due to: Eczema, Psoriasis, Seborrheic dermatitis, Insect bites, Rashes, Poison ivy, oak or sumac. Contact dermatitis caused by detergents and soaps, Cosmetics, Jewelry.
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.
Source
Official Health Canada record, licence 80003628
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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