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Founded in:
1999-12-22 -
Country:
China -
Address:
Tangshan Guye District Linxi Hexilixi -
Tax NO.:
9113020072161079XW -
Registered Funds:
12.9 million yuan -
Email:
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Urea |
It can dissolve and denature skin keratin, increase hydration of the stratum corneum, thereby making the skin soft and preventing it from drying out.
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It can dissolve and denature skin keratin, increase hydration of the stratum corneum, thereby making the skin soft and preventing it from drying out. |
150mg | 57-13-6 | 18 |
| Vitamin E |
It is an antioxidant that can maintain the normal development and function of muscles and nerves
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It is an antioxidant that can maintain the normal development and function of muscles and nerves |
10mg | 2074-53-5 | 11 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Miconazole nitrate |
This product is a broad-spectrum antifungal drug. Its mechanism of action is to inhibit the synthesis of fungal cell membranes and affect their metabolic processes. It has antibacterial effects on dermatophytes, Candida, etc., and also has a certain effect on some Gram-positive cocci.
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This product is a broad-spectrum antifungal drug. Its mechanism of action is to inhibit the synthesis of fungal cell membranes and affect their metabolic processes. It has antibacterial effects on dermatophytes, Candida, etc., and also has a certain effect on some Gram-positive cocci. |
0.02g | 22832-87-7 | 31 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Miconazole nitrate |
Imidazole antifungal drugs have antibacterial effects and can also have bactericidal effects at high concentrations; they can inhibit the biosynthesis of fungal ergosterol and other sterols; they act on the fungal cell membrane, damaging the fungal cell membrane and changing its permeability, causing the leakage of important intracellular substances; they can also inhibit the biosynthesis of fungal triglycerides and phospholipids; they can also inhibit the activity of oxidation and peroxidase, causing excessive accumulation of peroxides in the cell, leading to degeneration or necrosis of the fungal subcellular structure; for Candida albicans, they can inhibit the transformation of its spores into invasive hyphae.
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Imidazole antifungal drugs have antibacterial effects and can also have bactericidal effects at high concentrations; they can inhibit the biosynthesis of fungal ergosterol and other sterols; they act on the fungal cell membrane, damaging the fungal cell membrane and changing its permeability, causing the leakage of important intracellular substances; they can also inhibit the biosynthesis of fungal triglycerides and phospholipids; they can also inhibit the activity of oxidation and peroxidase, causing excessive accumulation of peroxides in the cell, leading to degeneration or necrosis of the fungal subcellular structure; for Candida albicans, they can inhibit the transformation of its spores into invasive hyphae. |
22832-87-7 | 31 | |
| Clobetasol propionate |
A highly potent topical corticosteroid with capillary constriction and anti-inflammatory effects.
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A highly potent topical corticosteroid with capillary constriction and anti-inflammatory effects. |
25122-46-7 | 26 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Halcinonide |
A highly effective fluorinated and chlorinated corticosteroid with anti-inflammatory, antipruritic and vasoconstrictive effects. It increases the reactivity of β receptors to catecholamine, activates adenylate cyclase to increase CAMP production, and inhibits phosphoethylesterase to reduce CAMP destruction, resulting in an increase in cAMP concentration in cells and inhibiting the release of histamine. Its effect in inhibiting the proliferation of granulomas in rats and mice is similar to that of dexamethasone.
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A highly effective fluorinated and chlorinated corticosteroid with anti-inflammatory, antipruritic and vasoconstrictive effects. It increases the reactivity of β receptors to catecholamine, activates adenylate cyclase to increase CAMP production, and inhibits phosphoethylesterase to reduce CAMP destruction, resulting in an increase in cAMP concentration in cells and inhibiting the release of histamine. Its effect in inhibiting the proliferation of granulomas in rats and mice is similar to that of dexamethasone. |
3093-35-4 | 9 |