This product is a nucleoside antiviral drug that has a selective inhibitory effect on a variety of herpes viruses (HSV). After acyclovir enters HSV-infected cells, it binds to the specific thymidylate kinase encoded by the virus and is rapidly converted into acyclosine monophosphate, which is then converted into acyclosine diphosphate by the cell guanylate kinase, and then converted into acyclosine triphosphate by other cell enzymes, and competes with guanylate triphosphate to infect herpes simplex virus DNA polymerase, thereby inhibiting viral DNA synthesis. Acyclovir triphosphate is a strong viral DNA polymerase inhibitor, which has an inhibitory effect on the DNA polymerase of five human herpes viruses, namely HSV-1, HSV-2, VZV, CMZ and EBV, and has no effect on normal cells. Its antiviral efficacy is 160 times stronger than that of adenosine.

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.

A highly potent topical corticosteroid with capillary constriction and anti-inflammatory effects.

Antibiotic, antibacterial spectrum is similar to erythromycin, mainly has high antibacterial activity against Gram-positive bacteria, its mechanism of action is to inhibit bacterial protein synthesis.

Local anesthetic, external use has analgesic and antipruritic effects.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

It is a highly effective fluorinated and chlorinated corticosteroid with anti-inflammatory, anti-itching 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.