Advantages of Dardia®

Dardia® meets the most rigorous pharmaceutical standards, using high quality ingredients, test standards, and manufacture process. The advantages of Dardia® include:

  • Improvement of moisture content by inclusion of reliable pharmaceutical moisturisers (glycerin, lactate, urea) (See: Clinical Tests)
  • Minimum number of highly purified ingredients to maximise skin tolerance
  • No cosmetic frills (perfumes, preservatives, colorants, etc.)
  • High levels of lipid content for extra effectiveness
  • Safety on sensitive skin proven in clinical trials conforming to Good Clinical Practice (= GCP) (See: What is GCP/GMP?) proving its safety on sensitive skin.
  • Manufacturing according to pharmaceutical standards (Good Manufacturing Practice = GMP) (See: What is GCP/GMP?)

Excellent sensory properties

Dardia® products are pleasant to use and feel good:

  • Soothing on sore skin (not for use on open wounds)
  • Smoothing on rough skin
  • Easy to apply even over large areas

Dardia® products provide the hydration and occlusive effect of water-in-oil emulsions, while maintaining a positive sensory experience.

Dardia® Lipo Cream and Lipo Milk were evaluated by volunteers after 4 weeks of twice daily application to face and body. The Dardia® Lipo Cream was rated as good-to-excellent by 70 % of the volunteers, and 80 % rated Dardia® Lipo Milk good-to-excellent.

Dardia® Lipo Cream and Dardia® Lipo Milk both spread evenly, are easily absorbed, soothing on dry skin and have a neutral scent (no perfumes).


What is pharmaceutical quality?

The development and production of Dardia® are subject to many of the same standards of quality used for drugs within the pharmaceutical industry. Dardia® meets the following requirements:

  • Selection of pharmagrade raw materials
  • Quality audits of suppliers
  • Pharmaceutically controlled manufacturing (international standard: GMP) (See: What is GCP/GMP?)
  • Pharmaceutically controlled clinical testing (international standard: GCP) (See: What is GCP/GMP? )
  • Additional filtering of lipids during and following production
  • Permanent quality testing and assurance
  • Comprehensive documentation
  • Change control
  • No more than 15 raw material ingredients
  • Storage of products according to pharmaceutical specifications

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