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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 |
|---|---|---|---|---|
| Triamcinolone acetonide 21-acetate |
Adrenal glucocorticoid drugs. External use has anti-inflammatory, anti-allergic and antipruritic effects, and can eliminate fever, redness and swelling caused by local non-infectious inflammation.
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Adrenal glucocorticoid drugs. External use has anti-inflammatory, anti-allergic and antipruritic effects, and can eliminate fever, redness and swelling caused by local non-infectious inflammation. |
1mg | 3870-07-3 | 5 |
| Urea |
It can dissolve keratin, increase the hydration of protein, and has antipruritic and antibacterial effects, and can increase the penetration of drugs through the skin.
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It can dissolve keratin, increase the hydration of protein, and has antipruritic and antibacterial effects, and can increase the penetration of drugs through the skin. |
100mg | 57-13-6 | 18 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Clobetasol propionate |
This product acts quickly and is one of the most potent topical corticosteroids currently used in clinical practice. It has a strong capillary constriction effect, and its anti-inflammatory effect is 112.5 times that of hydrocortisone, 2.3 times that of betamethasone sodium phosphate, and 18.7 times that of fluocinolone. The systemic adverse reactions are 3 times that of fluocinolone, with no sodium retention effect, and a certain effect of promoting sodium and potassium excretion. After topical application, it can be absorbed through the intact skin. After absorption, it is mainly metabolized in the liver and excreted through the kidneys, just like the metabolism of systemically administered corticosteroids in the body.
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This product acts quickly and is one of the most potent topical corticosteroids currently used in clinical practice. It has a strong capillary constriction effect, and its anti-inflammatory effect is 112.5 times that of hydrocortisone, 2.3 times that of betamethasone sodium phosphate, and 18.7 times that of fluocinolone. The systemic adverse reactions are 3 times that of fluocinolone, with no sodium retention effect, and a certain effect of promoting sodium and potassium excretion. After topical application, it can be absorbed through the intact skin. After absorption, it is mainly metabolized in the liver and excreted through the kidneys, just like the metabolism of systemically administered corticosteroids in the body. |
25122-46-7 | 27 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Ribavirin |
Antiviral drug. It has the effect of inhibiting the growth of many viruses such as respiratory syncytial virus, influenza virus, hepatitis A virus, adenovirus, etc. in vitro, and its mechanism is not fully understood. This product does not change the adsorption, invasion and uncoating of viruses, nor does it induce the production of interferon. After entering the virus-infected cells, the drug is rapidly phosphorylated, and its product acts as a competitive inhibitor of viral synthase, inhibiting inosine monophosphate dehydrogenase, influenza virus RNA polymerase and mRNA guanosine transferase, thereby causing a decrease in intracellular guanosine triphosphate, impairing viral RNA and protein synthesis, and inhibiting viral replication and transmission. It may also have an immune effect and neutralizing antibody effect on respiratory syncytial virus.
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Antiviral drug. It has the effect of inhibiting the growth of many viruses such as respiratory syncytial virus, influenza virus, hepatitis A virus, adenovirus, etc. in vitro, and its mechanism is not fully understood. This product does not change the adsorption, invasion and uncoating of viruses, nor does it induce the production of interferon. After entering the virus-infected cells, the drug is rapidly phosphorylated, and its product acts as a competitive inhibitor of viral synthase, inhibiting inosine monophosphate dehydrogenase, influenza virus RNA polymerase and mRNA guanosine transferase, thereby causing a decrease in intracellular guanosine triphosphate, impairing viral RNA and protein synthesis, and inhibiting viral replication and transmission. It may also have an immune effect and neutralizing antibody effect on respiratory syncytial virus. |
36791-04-5 | 33 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Salicylic acid |
Keratin dissolving softener with antibacterial and antipruritic effects
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Keratin dissolving softener with antibacterial and antipruritic effects |
44mg | 69-72-7 | 10 |
| Benzoic acid |
Preservative, has a weak antibacterial effect
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Preservative, has a weak antibacterial effect |
60mg | 65-85-0 | 15 |
| Pinitol oil |
Antipruritic, astringent, keratin dissolving and antibacterial effects
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Antipruritic, astringent, keratin dissolving and antibacterial effects |
0.3ml | 8002-09-3 | 0 |
| Ethanol |
The benzoic acid contained in this product is a preservative with a weak antibacterial effect; salicylic acid is a keratin dissolving and softening agent, and has antibacterial and antipruritic effects. Pine distillate oil has antipruritic, astringent, keratin dissolving and antibacterial effects.
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The benzoic acid contained in this product is a preservative with a weak antibacterial effect; salicylic acid is a keratin dissolving and softening agent, and has antibacterial and antipruritic effects. Pine distillate oil has antipruritic, astringent, keratin dissolving and antibacterial effects. |
64-17-5 | 90 |
| Name | Description | Content | CAS NO. | Registered Holders |
|---|---|---|---|---|
| Clotrimazole |
Clotrimazole is an azole antifungal drug. It can inhibit the process of Candida albicans transforming from spores to invasive hyphae. Clotrimazole has a broad-spectrum antifungal activity. It has good antibacterial effects on Epidermophyton, Trichophyton, Aspergillus, Chromatid fungi, Cryptococcus and Candida. It also has certain antibacterial activity against Sporothrix schenckii, Blastomyces dermatitidis, Coccidioides and Histoplasma. Clotrimazole has poor effects on Aspergillus, some dark spores, Mucor and other genus. This product inhibits the biosynthesis of fungal ergosterol and other sterols by interfering with the activity of cytochrome P-450, damaging the fungal cell membrane and changing its permeability, resulting in the leakage of important intracellular substances; it can inhibit the biosynthesis of fungal triglycerides and phospholipids; it can also inhibit the activity of oxidases and peroxidases, causing the accumulation of hydrogen peroxide in cells, leading to cell submicrostructure degeneration and cell necrosis.
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Clotrimazole is an azole antifungal drug. It can inhibit the process of Candida albicans transforming from spores to invasive hyphae. Clotrimazole has a broad-spectrum antifungal activity. It has good antibacterial effects on Epidermophyton, Trichophyton, Aspergillus, Chromatid fungi, Cryptococcus and Candida. It also has certain antibacterial activity against Sporothrix schenckii, Blastomyces dermatitidis, Coccidioides and Histoplasma. Clotrimazole has poor effects on Aspergillus, some dark spores, Mucor and other genus. This product inhibits the biosynthesis of fungal ergosterol and other sterols by interfering with the activity of cytochrome P-450, damaging the fungal cell membrane and changing its permeability, resulting in the leakage of important intracellular substances; it can inhibit the biosynthesis of fungal triglycerides and phospholipids; it can also inhibit the activity of oxidases and peroxidases, causing the accumulation of hydrogen peroxide in cells, leading to cell submicrostructure degeneration and cell necrosis. |
23593-75-1 | 45 |