A kind of medicinal composition for acne
A composition and drug technology, applied in the directions of drug combination, pharmaceutical formula, plant raw materials, etc., can solve the problems of pigmentation, easy recurrence, poor drug safety, etc., and achieve the effects of short course of treatment, good therapeutic effect, and no toxic side effects.
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Embodiment 1
[0026] A pharmaceutical composition for acne, characterized in that it is prepared from the following raw materials in weight ratio,
[0027] 40 parts of white peony, 30 parts of loquat leaves, 30 parts of uncaria, 30 parts of kudzu root, 30 parts of rhodiola,
[0028] 27 parts of rhubarb, 27 parts of cinnamon, 25 parts of frankincense, 25 parts of myrrh, 25 parts of cistanche,
[0029] 20 parts of Lycium barbarum, 20 parts of Caulis Spatholobus, 20 parts of Citrus aurantium, 18 parts of Poria cocos, 18 parts of Polygonatum odoratum,
[0030] 15 parts of Alisma, 15 parts of Cao Guo, 15 parts of cassia seed, 10 parts of dandelion, 10 parts of plantain seed,
[0031] Codonopsis 10, Licorice 5, Lily 5, Imperata 5, Chuanxiong 3.
[0032] Its preparation method is as follows:
[0033] (1) Weigh the raw materials according to the parts by weight for later use.
[0034] (2) Take uncaria, kudzu root, rhodiola rosea, millet root, citrus aurantium, poria, polygonatum, grass fruit, c...
Embodiment 2
[0041] clinical information
[0042] standard constrain:
[0043]1) Age 18-45 years old, both male and female. 2) The onset begins at puberty, and it tends to occur on the face, upper chest and back where the sebaceous glands are developed, and the distribution is symmetrical. The skin lesions are follicular papules, pustules, nodules, cysts, comedones, and scars, with seborrhea and a chronic course. 3) The patient is able to complete the trial and voluntarily signs a written informed consent before the trial begins. 4) Those who have not used too much internal medicine or photosensitive drugs related to the disease within 30 days before treatment;
[0044] This trial was carried out in 4 clinical centers in China, and a total of 99 subjects were randomly enrolled. 45 male subjects and 54 female subjects were randomly divided into two groups, wherein the control group: 50 cases, and the experimental group: 49 cases. The control group was given minocycline hydrochloride cap...
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