Medical aesthetics - Exposure detox mask

PRODUCT DETAILED INFORMATION

exposure® detox mask

DESCRIPTION
Exposure® Detox Mask is a dermatological antioxidant complex with natural inositol phosphates. It introduces a unique delivery system, based on convenient single use masks that can be activated in seconds (for external use only).

MAIN INGREDIENTS
Aqua, propylene glycol, butylene glycol, peg-60 hydrogenated castor oil, citrus medica limonum, pyrus malus, prunus persica, triticum vulgare, hordeum vulgare, panax ginseng, methylcholoisithiazolinone, methylisothiazolinone, soduim hydroxide, phenoxyethanol.

INDICATIONS
The powerful formulation of Exposure® Detox Mask contains exclusively botanical active ingredients. Its use is recommended for regular skin protection against environmental stress and toxic substances, and to soothe and regenerate sensitive or irritated skin.
Specially recommended after sunbathing, shaving, epilation, chemical peels, and laser / ipl / radiofrequency treatments.

PROPERTIES
Exposure® Detox Mask fights the effects of environmental stresses that can damage the skin and accelerate tissue ageing and photodamage. Its unique formulation uses only natural active ingredients, providing advanced results at four levels:

neutralization of environmental heavy metals from pollution: provided by wheat and barley germ’s inositol phosphate.
antioxidation against free radicals, unstable molecules directly involved in the skin ageing process : provided by panax ginseng
protection of skin cell membranes, avoiding lipoperoxidation: provided by lemon, apple and peach extracts.
soothing and calming: provided by natural plant and fruit extract

DIRECTIONS
Suitable for all skin types (topical use only). To activate a mask:

1. Pour the contents of one vial on the container provided and then drop one of the white cellulose tablets on it.

2. Allow a few seconds for the cellulose tablet to absorve the fluid.

3. Remove any excess fluid. Gently unfold the mask. The mask is activated and ready to be applied.

4. Leave the mask in direct contact with the skin at least 5 minutes. Repeat the previous steps once the mask becomes inactive using the remnant fluid in the container.

For optimum results, it is recommended to use once a week for the first month and then once every four weeks.

WARNING
Topical use only. Do not apply to eyes, mucose membranes and/or open wounds.
Some patients experience breakouts any time they change their skin care regimen. Skin reactions to any new topical product, though rare, are likely to occur within the first few days of use. If any reaction occurs, wash the product off and discontinue use.

CONTRAINDICATIONS
Prior history of sensitivity or allergic reaction to this product or any of its ingredients.

ADVERSE REACTIONS
No systemic adverse reactions have been reported. In rare cases, hypersensitivity (localized contact dermatitis) may occur: mask application should be discontinued and the physician notified immediately.

KEEP OUT OF THE REACH AND SIGHT OF CHILDREN

Not tested on animals
Manufactured in the EC for Medical Aesthetics Ltd., London, UK

BIBLIOGRAPHY
1. Tracking toxins. Biomonitoring outshines the indirect assessment of exposure in determining which pollulants enter the body, and whether they cause disease or disability. Murdock BS. EMBO Rep. 2005 Aug;6(8):701-5.
2. Total zinc absorption in young women, differs between vegetarian and meat-based diets with equal phytic acid content. Kristensen MB, Hels O, Morberg CM, Marving J, Bugel S, Tetens I. Br J Nutr. 2006
3. Absorption of zinc and retention of calcium: dose-dependent inhibition by phytate. Fredlund K, Isaksson M, Rossander-Hulthen L, Almgren A, Sandberg AS. J Trace Elem Med Biol. 2006;20(1):49-57. Epub 2006 Mar 2.
4. Study of the absorption of myo-inositol hexakisphosphate (InsP6) through the skin. Grases F, Perello J, Isern B, Prieto RM. Biol Pharm Bull. 2005 Apr;28(4):764-7.
5. The role of intracellular zinc in chromium(VI)-induced oxidative stress, DNA damage and apoptosis. Rudolf E, Cervinka M. Chem Biol Interact.
2006 Jun 27.
6. Green tea and the skin. Hsu S. J Am Acad Dermatol. 2005 Jun;52
(6):1049-59.
7. Molecular mechanisms underlying anti-tumor promoting activities of heat-processed Panax ginseng C.A. Meyer. Surh YJ, Na HK, Lee JY, Keum YS. J Korean Med Sci. 2001 Dec;16 Suppl:S38-41.
8. Cupric keratosis: green seborrheic keratoses secondary to external copper exposure. Peterson J, Shook BA, Wells MJ, Rodriguez M. Cutis. 2006 Jan;77(1):39-41.
9. Trace elements and melanoma. Bergomi M, Pellacani G, Vinceti M, Bassissi S, Malagoli C, Alber D, Sieri S, Vescovi L, Seidenari S, Vivoli R. J Trace Elem Med Biol. 2005;19(1):69-73.
10. Percutaneous absorption of inorganic lead compounds. Sun CC, Wong TT, Hwang YH, Chao KY, Jee SH, Wang JD. AIHA J (Fairfax, Va). 2002 Sep-Oct;63(5):641-6.
11. Environmental exposure to trace elements and risk of cutaneous melanoma. Vinceti M, Bassissi S, Malagoli C, Pellacani G, Alber D, Bergomi M, Seidenari S. J Expo Anal Environ Epidemiol. 2005 Sep;15(5):458-62.
12. Antipruritic effect of ginsenoside rb1 and compound k in scratching behavior mouse models. Shin YW, Kim DH. J Pharmacol Sci. 2005 Sep;99(1):83-8. Epub 2005 Sep.
13. Ginsenoside F1 protects human HaCaT keratinocytes from ultraviolet-B-induced apoptosis by maintaining constant levels of Bcl-2. Lee EH, Cho SY, Kim SJ, Shin ES, Chang HK, Kim DH, Yeom MH, Woe KS, Lee J, Sim YC, Lee TR. J Invest Dermatol. 2003 Sep;121(3):607-13.

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