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PRODUCT DETAILED INFORMATION
exposure® dermatological aloe vera gel
aloe vera
 

DESCRIPTION
Exposure® Dermatological Aloe Vera Gel with 95% aloe vera and camomile has soothing, decongestant, refreshing and regenerative skin properties (for external use only).

MAIN INGREDIENTS
Aloe barbadensis, aqua, dimethicone, chamomilla recutita oil, acrylates, sodium hydroxide, disodium edta, propylene glycol alginate, diazolidinyl urea, ci 42.051, ci 19.140.

INDICATIONS
Treatment of skin inflammation and irritation due to the following:

  • sunburn
  • sunbeds
  • chemical peels
  • laser / ipl / radiofrequency skin treatments
  • botulinum toxin / dermal fillers injections
  • microdermabrasion

and in general to soothe, moisturise and stimulate skin healing.

PROPERTIES
Exposure® Dermatological Aloe Vera Gel uses a patented original formula. The combination of a high concentration of aloe vera (95%) and camomile’s bisabolol provides:

  • analgesic properties (soothing and pain relief)
  • anti-inflammatory properties
  • antiseptic properties (antiviral, antifungal and antibacterial)
  • intensive moisturising properties
  • protective antioxidant effect against free radicals
  • skin repair

DIRECTIONS
Suitable for all skin types. Apply gently to affected areas as often as required, or as directed by your Doctor.
Exposure® Dermatological Aloe Vera Gel is suitable for use in face and body.

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 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.

 

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. An evaluation of the biological and toxicological properties of Aloe barbadensis (miller), Aloe vera. Boudreau MD, Beland FA. J Environ Sci Health C Environ Carcinog
2. Aloe vera: a valuable ingredient for the food, pharmaceutical and cosmetic industries. Eshun K, He Q. Crit Rev Food Sci Nutr. 2004;44(2):91-6.
3. Evaluation of antioxidant potential of aloe vera (Aloe barbadensis miller) extracts. Hu Y, Xu J, Hu Q. J Agric Food Chem. 2003 Dec 17;51(26):7788-91.
4. Aloe vera leaf gel: a review update. Reynolds T, Dweck AC.J Ethnopharmacol. 1999 Dec 15;68(1-3):3-37.
5. The Aloe vera phenomenon: a review of the properties and modern uses of the leaf parenchyma gel. Grindlay D, Reynolds T. J Ethnopharmacol. 1986 Jun;16(2-3):117-51.
6. Novel bioactive maloyl glucans from aloe vera gel: isolation, structure elucidation and in vitro bioassays. Esua MF, Rauwald JW. Carbohydr Res. 2006 Feb 27;341(3):355-64. Epub 2005 Dec 15.
7. Aloe vera. Klein AD, Penneys NS. J Am Acad Dermatol. 1988 Apr;18(4 Pt 1):714-20. Review. Erratum in: J Am Acad Dermatol 1988 Jul;19(1 Pt 1):82
8. Wound healing. Oral and topical activity of Aloe vera. Davis RH, Leitner MG, Russo JM, Byrne ME.
9. Phase III double-blind evaluation of an aloe vera gel as a prophylactic agent for radiation-induced skin toxicity. Williams MS, Burk M, Loprinzi CL, Hill M, Schomberg PJ, Nearhood K, O'Fallon JR, Laurie JA, Shanahan TG, Moore RL, Urias RE, Kuske RR, Engel RE, Eggleston WD. Int J Radiat Oncol Biol Phys. 1996 Sep 1;36(2):345-9.
10. Aloe vera: a systematic review of its clinical effectiveness. Vogler BK, Ernst E.
11. Isolation and characterization of active compounds from Aloe vera with a possible role in skin protection. Kostalova D, Bezakova L, Oblozinsky M, Kardosova A. Ceska Slov Farm. 2004 Sep;53(5):248-51. Slovak.

©2006 Medical Aesthetics Ltd. London (UK) All rights reserved

 

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