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  2. Monobenzone - Wikipedia

    en.wikipedia.org/wiki/Monobenzone

    Monobenzone, also called 4-(Benzyloxy)phenol and monobenzyl ether of hydroquinone (MBEH) is an organic chemical in the phenol family with chemical formula C 6 H 5 CH 2 OC 6 H 4 OH. [1] [2] It is used as a topical drug for medical depigmentation. [3] It is a colourless solid that is classified as the monobenzyl ether of hydroquinone.

  3. Hydroquinone - Wikipedia

    en.wikipedia.org/wiki/Hydroquinone

    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.

  4. Fluocinolone/hydroquinone/tretinoin - Wikipedia

    en.wikipedia.org/wiki/Fluocinolone/hydroquinone/...

    Fluocinolone acetonide (0.01%)/Hydroquinone (4%)/ Tretinoin (0.05%) Cream is indicated for the short-term (up to 8 weeks) treatment of moderate to severe melasma of the face in the presence of measures for sun avoidance, including the use of sunscreens.

  5. Esoterica (medication) - Wikipedia

    en.wikipedia.org/wiki/Esoterica_(medication)

    Esoterica is an over-the-counter topical ointment applied to the skin for the purpose of lightening freckles, age spots, chloasma, melasma, and other skin discolorations due to a benign localized increase in the production of melanin.

  6. Skin whitening - Wikipedia

    en.wikipedia.org/wiki/Skin_whitening

    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]

  7. Quinone - Wikipedia

    en.wikipedia.org/wiki/Quinone

    Quinones undergo addition reaction to form 1,4-addition products. [10] An example of 1,4-addition reaction is the addition of hydrogen chloride to form chlorohydroquinone: 1,4-addition reaction of quinone with hydrogen chloride to produce chlorohydroquinone. Quinones can undergo Diels–Alder reactions. [10]

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