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MEDICINAL FORMS powder 2.5g powder for the preparation of oral solution 2.5g. is a medicine factory.
GROUP The group of ascorbic acid (vitamin C)
COMPOSITION Active ingredient –

PHARMACOLOGICAL ACTION Replenishing vitamin C deficiency, metabolic, regulating redox processes, antioxidant. It is absorbed in the small intestine (duodenum, partially in the ileum). It is excreted in urine, feces, sweat, breast milk. Smoking and drinking ethyl alcohol accelerate destruction, drastically reducing body reserves.

It has pronounced antioxidant properties.

Regulates the transport of hydrogen in many biochemical reactions, improves the use of glucose in the tricarboxylic acid cycle, participates in the formation of tetrahydrofolic acid and tissue regeneration, the synthesis of steroid hormones, collagen, and collagen. Maintains normal capillary permeability. It activates proteolytic enzymes, participates in the exchange of aromatic amino acids, pigments and cholesterol, and contributes to the accumulation of glycogen in the liver. It improves bile secretion, restores exocrine pancreatic function and endocrine – thyroid function. Regulates immunological reactions, promotes phagocytosis, and increases the body’s resistance to infections.

It has anti-inflammatory and anti-allergic effects. FOR APPLICATION Hypovitaminosis C, hemorrhagic diathesis, capillarotoxicosis, hemorrhagic stroke, bleeding (nasal, pulmonary, uterine, etc.) infectious diseases, intoxications, alcoholic and infectious delirium, acute radiation sickness, post-transfusion complications, liver diseases (Botkin’s disease chronic hepatitis and cirrhosis), gastrointestinal tract (achilia, peptic ulcer, especially after bleeding, enteritis, colitis, helminthiasis), cholecystitis, adrenal insufficiency (Addison’s disease), sluggishly healing wounds, ulcers, ohms bones dystrophy, mental and physical overload, pregnancy and lactation, hemosiderosis, melasma, erythroderma, psoriasis, chronic common dermatoses.

As an antioxidant – atherosclerosis, bronchial asthma, diffuse connective tissue diseases.

ADVERSE EFFECTS Irritation of the gastrointestinal mucosa (nausea, vomiting, diarrhea), arterial hypertension, metabolic impairment, inhibition of the pancreatic insular apparatus (hyperglycemia, glucosuria) and glycogen synthesis, reduces capillary permeability and worsening tissue trophism, thrombocytopenia, hypertrombocytosis, hypertrombocytosis, neutrophilic leukocytosis, myocardial dystrophy, damage to the glomerular apparatus of the kidneys, allergic reactions (including anaphylactic shock); with prolonged use, the formation of urinary stones, impaired metabolism of zinc, copper, increased CNS excitability, sleep disturbance, the development of microangiopathies.

INTERACTION Increases the concentration in the blood of salicylates (increases the risk of crystalluria), ethinyl estradiol, benzylpenicillin and tetracyclines, and reduces oral contraceptives.

Reduces the anticoagulant effect of coumarin derivatives. Improves intestinal absorption of iron preparations. Increases total Cl of ethyl alcohol. Quinoline drugs, calcium chloride, salicylates, corticosteroids, with prolonged use, deplete vitamin C.

DOSAGE AND ADMINISTRATION Inside, after a meal. 
SPECIAL INSTRUCTIONS For effective treatment, monitoring of renal function, blood pressure and glucose level is necessary (especially when prescribing high doses)., as a reducing agent, can distort the results of various laboratory tests (blood glucose, bilirubin, transaminase activity, LDH).
STORAGE CONDITIONS In a dry, dark place at room temperature.