Products

Clotrimazole, an imidazole derivative with a broad spectrum of antimycotic activity. It inhibits the fungal lanosterol 14-alpha-demethylase which thereby prevents the formation of ergosterol, an essential component in the fungal cell membrane, resulting in increased cellular permeability.

Metronidazole, a synthetic antibacterial and antiprotozoal agent of the nitroimidazole class, is a prodrug. Unionized metronidazole is selective for anaerobic bacteria due to their ability to intracellularly reduce metronidazole to its active form. This reduced metronidazole then covalently binds to DNA, disrupt its helical structure, inhibiting bacterial nucleic acid synthesis and resulting in bacterial cell death.

Lactobacillus acidophilus is a bacteria that exists naturally in the body, primarily in the digestive, urinary, and genital systems. Also called as “friendly bacteria”.

Clotrimazole, is an imidazole derivative with a broad spectrum of antimycotic activity. It inhibits the fungal lanosterol 14-alpha-demethylase which thereby prevents the formation of ergosterol, an essential component in the fungal cell membrane, resulting in increased cellular permeability.

Diloxanide furoate is an anti-protozoal drug.

A synthetic tetracycline derivative with similar antimicrobial activity is used to inhibit bacterial protein synthesis.

Fluconazole, a synthetic antifungal agent of the imidazole class. It inhibits the fungal lanosterol 14-alpha-demethylase which thereby prevents the formation of ergosterol, an essential component in the fungal cell membrane, resulting in increased cellular permeability.

A semi-synthetic macrolide antibiotic of the azalide class. Azithromycin binds to the 50S subunit of the 70S bacterial ribosomes, and therefore inhibits RNA-dependent protein synthesis in bacterial cells.

Fluconazole, a synthetic antifungal agent of the imidazole class. It inhibits the fungal lanosterol 14-alpha-demethylase which thereby prevents the formation of ergosterol, an essential component in the fungal cell membrane, resulting in increased cellular permeability.

Broad spectrum antifungal agent. It inhibits the fungal lanosterol 14-alpha-demethylase which thereby prevents the formation of ergosterol, an essential component in the fungal cell membrane.

A synthetic fluoroquinolone (fluoroquinolones) antibacterial agent that inhibits the supercoiling activity of bacterial DNA gyrase, halting DNA replication.

A lincosamide antibiotic, which inhibits protein synthesis in susceptible bacteria by binding to the 50 S subunits of bacterial ribosomes and preventing peptide bond formation upon transcription.

Metronidazole, a synthetic antibacterial and antiprotozoal agent of the nitroimidazole class, is a prodrug. Unionized metronidazole is selective for anaerobic bacteria due to their ability to intracellularly reduce metronidazole to its active form. This reduced metronidazole then covalently binds to DNA, disrupt its helical structure, inhibiting bacterial nucleic acid synthesis and resulting in bacterial cell death.

Metronidazole, a synthetic antibacterial and antiprotozoal agent of the nitroimidazole class, is a prodrug. Unionized metronidazole is selective for anaerobic bacteria due to their ability to intracellularly reduce metronidazole to its active form. This reduced metronidazole then covalently binds to DNA, disrupt its helical structure, inhibiting bacterial nucleic acid synthesis and resulting in bacterial cell death.

Metronidazole, a synthetic antibacterial and antiprotozoal agent of the nitroimidazole class, is a prodrug. Unionized metronidazole is selective for anaerobic bacteria due to their ability to intracellularly reduce metronidazole to its active form. This reduced metronidazole then covalently binds to DNA, disrupt its helical structure, inhibiting bacterial nucleic acid synthesis and resulting in bacterial cell death.

Clotrimazole, an imidazole derivative with a broad spectrum of antimycotic activity. It inhibits the fungal lanosterol 14-alpha-demethylase which thereby prevents the formation of ergosterol, an essential component in the fungal cell membrane, resulting in increased cellular permeability.

Lactobacillus acidophilus is a bacteria that exists naturally in the body, primarily in the digestive, urinary, and genital systems. Also called as “friendly bacteria”.

Nalidixic acid is a quinolone antibacterial agent, binds strongly, but reversibly, to DNA, interfering with synthesis of RNA and, consequently, with protein synthesis.

Norfloxacin is a synthetic fluoroquinolone (fluoroquinolones) with broad-spectrum antibacterial activity, blocks bacterial DNA replication by binding itself to an enzyme called DNA gyrase.

Metronidazole, a synthetic antibacterial and antiprotozoal agent of the nitroimidazole class, is a prodrug. Unionized metronidazole is selective for anaerobic bacteria due to their ability to intracellularly reduce metronidazole to its active form. This reduced metronidazole then covalently binds to DNA, disrupt its helical structure, inhibiting bacterial nucleic acid synthesis and resulting in bacterial cell death.

A synthetic fluoroquinolone (fluoroquinolones) antibacterial agent that inhibits the supercoiling activity of bacterial DNA gyrase, halting DNA replication.

Ornidazole is a 5-nitroimidazole derivative active against protozoa and anaerobic bacteria. Interact with DNA to cause destruction of helical DNA structure and strand leading to a protein synthesis inhibition and cell death in susceptible organisms.

Ornidazole is a 5-nitroimidazole derivative active against protozoa and anaerobic bacteria. Interact with DNA to cause destruction of helical DNA structure and strand leading to a protein synthesis inhibition and cell death in susceptible organisms.

Trimethoprim is a pyrimidine analogue that disrupts folate synthesis, by inhibiting dihydrofolate reductase. Inhibition of the enzyme starves the bacteria of nucleotides necessary for DNA replication.
Sulfamethoxazole is a sulfonamide drug that inhibits bacterial synthesis of dihydrofolic acid.

Ambroxol is a secretolytic agent used in the treatment of respiratory diseases associated with viscid or excessive mucus. It stimulates synthesis and release of surfactant by type II pneumocytes that acts as an anti-glue factor by reducing the adhesion of mucus to the bronchial wall, in improving its transport and in providing protection against infection and irritating agents.

Salbutamol is a beta (2)-adrenergic agonist that results in relaxation of bronchial smooth muscles by binding to beta (2)-receptors in the lungs.

A histamine H1 antagonist, Chlorpheniramine blocks the action of endogenous histamine by binding to the histamine H1 receptor, which subsequently leads to temporary relief of the negative symptoms brought on by histamine.

Levocetirizine, an active isomer of cetirizine, selectively inhibits histamine H1-receptors

Paracetamol is an analgesic and antipyretic drug that acts primarily in the CNS, increasing the pain threshold by inhibiting cyclooxygenase, enzymes involved in prostaglandin (PG) synthesis.

Phenylephrine is a sympathomimetic amine that acts predominantly on α-adrenergic receptors working as a powerful vasoconstrictor.

A naturally occurring methylxanthine used as a pharmacological agent. Caffeine’s most notable pharmacological effect is as a central nervous system stimulant, also relaxes smooth muscle, stimulates cardiac muscle and stimulates diuresis.

A histamine H1 antagonist, Chlorpheniramine blocks the action of endogenous histamine by binding to the histamine H1 receptor, which subsequently leads to temporary relief of the negative symptoms brought on by histamine.

A potent second-generation histamine H1 antagonist, Cetirizine competes with histamine for binding at H1-receptor sites on the effector cell surface, resulting in suppression of histaminic edema, flare, and pruritus.

A second generation, tricyclic antihistamine, Desloratadine competes with free histamine for binding at H1-receptors in the GI tract, uterus, large blood vessels, and bronchial smooth muscle. This block the action of endogenous histamine, which subsequently leads to temporary relief from the negative symptoms brought on by histamine.