Purifying cleansing gel

A complete formula to clean and sanitise all kinds of irritations. This purifying and non-drying cleansing gel soothes and reduces irritation on the face, body, external intimate areas and scalp for 48 hours*.

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* Tolerance and efficacy study under dermatological, paediatric, gynaecological and ophthalmological control. 89 subjects, 1 application per day for 21 days.

  • For whom?
    Family
    From birth
  • Price
    200ml
    11,19€
  • Texture
    Blue texture
    foams on application

Patient relations

  • Application tips

    Apply once or twice a day to the irritated area. Lather and rinse. Wipe gently by dabbing the skin, without rubbing.

  • In combination with the following treatments

    Suitable for people undergoing anti-cancer treatment or post-treatment.

Ingredients

Active ingredients:

[C+-Restore]™
Ingredient C+Restore

[C+-Restore]™ is the first patented [patent filed] post-biotic repairing active ingredient from Avène Thermal Spring Water. Developed from a unique bacterium, it substantially promotes skin renewal.
 

Copper / Zinc
Actif Cuivre / Zinc

Antibacterial complex, limits the risk of bacterial proliferation.

Formula details:

AVENE THERMAL SPRING WATER (AVENE AQUA)
WATER
GLYCERIN
DISODIUM COCO-GLUCOSIDE CITRATE
DECYL GLUCOSIDE
SODIUM COCOAMPHOACETATE
PENTYLENE GLYCOL
AQUAPHILUS DOLOMIAE FERMENT FILTRATE
ARGININE
CITRIC ACID
COPPER SULFATE
SODIUM CHLORIDE
TRISODIUM ETHYLENEDIAMINE DISUCCINATE
TROMETHAMINE
XANTHAN GUM
ZINC SULFATE

Click on an ingredient type to highlight it in the list

Active ingredient
Water
Cleaner
Stabilizing agent
PH regulator
Texturing agent

Clinical results and publications

Efficacy results

1

Sanitises (1) and removes bacteria in just one wash

94%

Immediately soothes feelings of discomfort (2)

48H

Improves irritation after 48 hours (2)

Legal Notice

(1) In-vitro study, evaluation of the purifying effect on representative germs of the skin.


(2) Tolerance and efficacy studies under dermatological, paediatric, gynaecological and ophthalmological control. 89 subjects, 1 application per day for 21 days.

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