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Dermone Skincare, formally SophytoPRO, was researched and developed by Cosmetic Research Laboratories, a British research company who have been championing green technology since their humble beginnings in 2000. They have won numerous innovation awards, have been mentioned in New York Times bestsellers authored by doctors and its owners were honored to represent the UK Soil Association as Goodwill Ambassadors in the US.
Over the years Cosmetic Research Laboratories have worked passionately to innovate and create clinically effective, plant-based formulas and patent-pending extracts; expanding to where their technology is now found in many well known names in health and beauty. DermOne Skincare is designed exclusively for Healthcare Practitioners and is distributed throughout North America.
SPECIALIZATION: Reprofiling skin micribiome using patent-pending technology, phytotherapy and other specialty ingredients.
INGREDIENT STANDARDS: Having worked to EU Cosmetics Regulation (EC) No 1223/2009 since 2000, we're no stranger to rigorous standards. This ensures ingredients meet restrictions set forth by these regulations for product and ingredient safety assessments. It lists all substances that must not be used owing to their toxicity, substances that can only be used in special circumstances and the substances approved for use in cosmetics like coloring agents, preservatives and UV filters. Additionally, all cosmetic labels must carry the standardized INCI (International Nomenclature of Cosmetic Ingredient) name for each ingredient. This allows the consumer to easily compare ingredients between different products, using a common language.
GOOD MANUFACTURING PRACTICES (GMP): We manufacture our products in both British and American facilities. Our British location is certified to handle organic ingredients by both the UK Soil Association and the USDA. We adhere to ISO 9001:2008, ISO 22716:2008 (GMP) good manufacturing principles as laid out in the Official Journal of the European Union. Our US facility is FDA-registered (Food & Drug Administration) for OTC (over-the-counter) drugs and in full compliance with currant good manufacturing practice (cGMP) guidelines 21 CFR part 210 and 211.
CLAIMS: The EU Cosmetics Regulation sets the principles for claims that manufacturers can make on their packaging. This is complemented by the common criteria on claims regulation and guidelines that outline how claims should be made.