DEXYANE MeD Palpebral

Medical device

Treats eczema lesions - Soothes - Soothes itchiness - Decongests

A medical device that treats atopic or contact eczema on the eyelids.

Soothes and reduces the reactivity of sensitive, atopy-prone eyelids

Soothes and reduces the reactivity of atopy-prone eyelids. Tested under dermatological control.

Cannula tube

Usable by Infants - Children - Family - Adults

Age From 3 month(s)

Suitable Eyelids

Skin type Eyelid atopy

Need Anti-eczema

Made in France

Environmental impact

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Formula

Biodegradable formula*
Formulated to limit the impact on the aquatic environment***
85% of ingredients of natural origin
*According to a OECD 301 test or biodegradability index method
*** According to a OECD 301 test and CLP classification of the formula

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Packaging

Fully recyclable packaging

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Manufacturing

Manufactured and packaged in an environmentally certified facility****
****According to ISO 14001 and/or 50001

Societal impact

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Product manufactured and packaged in a factory with high social standards
Ducray is a brand of the Pierre Fabre Group, certified at the highest Exemplary level of AFNOR Certification’s Committed to CSR and Responsibility Europe labels, thus consolidating a long-standing commitment to contributing to sustainable development. ...

Application

Frequency of use

1 to 2 times a day

• Do not use the product if the tube is damaged
• If you experience any side effects as a result of using the product, seek medical advice
• Can be used on skin damaged by cancer treatments|• Apply a thin layer directly on the affected eyelids with a clean finger, avoiding contact with the eye
• For external use
• Use as a stand-alone treatment, in combination with, or as a follow-up to topical corticosteroids
• Once or twice a week
• Do not use if you are allergic to any of the ingredients
• If you experience an allergic reaction, consult a doctor
• Due to a lack of data, use if pregnant or breastfeeding is not recommended
• Keep out of the reach of children
• Avoid direct contact with the eyes
• Close the tube tightly after use
• Do not use the product if the tube is damaged
• If you experience any side effects as a result of using the product, seek medical advice
• Can be used on skin damaged by cancer treatments

• Apply a thin layer directly on the affected eyelids with a clean finger, avoiding contact with the eye
• For external use
• Use as a stand-alone treatment, in combination with, or as a follow-up to topical corticosteroids
• Once or twice a week
• Do not use if you are allergic to any of the ingredients
• If you experience an allergic reaction, consult a doctor
• Due to a lack of data, use if pregnant or breastfeeding is not recommended
• Keep out of the reach of children
• Avoid direct contact with the eyes
• Close the tube tightly after use
• Do not use the product if the tube is damaged
• If you experience any side effects as a result of using the product, seek medical advice
• Can be used on skin damaged by cancer treatments

Ingredients

Ingredients

WATER (AQUA). GLYCERIN. CAPRYLIC/CAPRIC TRIGLYCERIDE. BUTYLENE GLYCOL. POLYSORBATE 60. GLYCERYL STEARATE. BUTYROSPERMUM PARKII (SHEA) BUTTER. BEESWAX. PEG-100 STEARATE. 10-HYDROXYDECENOIC ACID. CAPRYLYL GLYCOL. CETYL ALCOHOL.CITRIC ACID. GLYCYRRHETINIC ACID. POLYACRYLATE-13. POLYISOBUTENE. POLYSORBATE 20. SCLEROTIUM GUM. SORBITAN ISOSTEARATE.

The consumer is advised to systematically check the composition of the product before purchasing it.

Results

• Immediately¹ after application : itching reduced.
• After 3 days¹ : significant improvement and even complete disappearance of clinical signs, particularly burning sensations.

¹Result of a clinical study conducted on 33 adults from 19-70 years old with mild to moderate atopic or contact eyelid eczema. DEXYANE MeD Palpebral was applied twice a day to the eyelids for 22 days. The clinical severity score (including itching, burning, tightness, etc.) from 0 to 9, immediately after 3 days of application, was compared to the pre-application scores. Immediately, the itching score significantly decreased, and the burning score improved by day 3. The overall development of lesions was evaluated by the PGA score on a 5-point scale : 0 (aggravation) to 4 (completely healed); after 3 days of application, the majority of patients felt an improvement. PFDC study PRM03-F-197_V3_AN. 03/2019. 98-104, 108.

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