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Hydroquinone is a commonly used agent in skin whiteners. The European Union banned it from cosmetics in 2000. [9] It works by decreasing melanin production. [9] Tretinoin, also known as all-trans retinoic acid, may be used to whiten specific areas. [6] It may be used in combination with steroids and hydroquinone. [6]
Hydroquinone, also known as benzene-1,4-diol or quinol, is an aromatic organic compound that is a type of phenol, a derivative of benzene, having the chemical formula C 6 H 4 (OH) 2. It has two hydroxyl groups bonded to a benzene ring in a para position.
[18] [19] Hydroquinone was the most commonly prescribed hyperpigmentation treatment before the long-term safety concerns were raised, [20] and the use of it became more regulated in several countries and discouraged in general by WHO. [21] For the US, only 2% is at present sold over-the-counter, and 4% needs prescription.
Two carcinogenic chemicals used in cleaning products and other common household goods have been banned in the U.S., the Environmental Protection Agency (EPA) announced in a Dec. 9 press release.
Hydroquinone is the compound most frequently used in skin-whitening products. Due to concerns about its side effects, it was almost banned by the FDA in 2006, as medical issues of carcinogenicity and reports of disfiguring ochronosis existed. [10] In the European Union hydroquinone has been banned in cosmetic creams since 2000. [11]
This wrinkly legume from South America underwent a recent boom in the fine-dining world due to its notes of vanilla, almond, and cinnamon, but it has actually been illegal in the U.S. since 1954.
The amendment banned production, sale and transportation of liquor; but consumption was allowed. One year after ratification, on January 17, 1920, Prohibition began.
[17]: 12 Reintroduced as a dietary supplement in 2006; [17]: 13 in 2013 the FDA started work to ban it due to cardiovascular problems [18] Dinoprostone: 1990 UK Uterine hypotonus, fetal distress. [3] Dipyrone 1975 UK, US, Others Agranulocytosis, anaphylactic reactions. [3] Dithiazanine iodide: 1964 France, US