CompoAtlas

Gengigel Teething

Natural health product licensed in Canada

Licence holder
Ricerfarma S.R.L.
NPN or DIN-HM
80072962
Status
Active licence
Licence date
11 October 2016
Revision date
Not provided
Form
Gel gingivale
Route of administration
Gingivale
Application type
Non traditionnelle

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

Composition

Medicinal ingredient and sourcePer dosage unit, according to the source
Acide hyaluronique

Source : Streptococcus equi - capsule extracellulaire bactérienne

0.54 %

Non-medicinal ingredients

Eau, Lactate de sodium, Hydroxyde de sodium, Poly(alcool vinylique), VP/Eicosene Copolymer, Lécithine, Polycarbophil, xylitol, Gomme de cellulose, Polyvinylpyrrolidone, Laurate de glycéryle, Edetate Disodium, Saccharine, Huile de ricin hydrogénée de PEG-40, Tribasic sodium phosphate, Phosphate de sodium, monobasique, PVM/MA Copolymer, Polyéthylène glycol, mono(p-nonylphényl) éther, ramifié, Acide lactique

PopulationAgeQuantity per servingFrequency
Enfantsminimum: 1 year ; maximum: 3 years3 millilitreminimum: 3 Tous les jours ; maximum: 6 Tous les jours

Uses authorised in Canada

Aide à soulager la douleur, la rougeur et à réduire l'inflammation des gencives causées par la poussée des premières detns.

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 80072962

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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