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Biologically Active Food Supplement (Dietary Supplement), Which Is An Additional Source Of 13 Vitamins And 14 Minerals For Adults, In The Form Of Tablets Weighing Strictly 1455 Mg, Coated With The Original Film Coating Opadry Ii White (Containing Hydroxypropyl Methylcellulose, Titanium Dioxide, Polydextrose, Talc, Maltodextrin, Medium Chain Triglycerides), Containing Calcium Phosphate In Each Tablet Dibasic Anhydrous, Magnesium Oxide, Potassium Chloride, Vitamin C (L-Ascorbic Acid), Ferric Fumarate, Vitamin E (D-Alpha Tocopherol Acetate), Niacinamide, Zinc Oxide, Vitamin B5 (Calcium D-Pantothenate), Vitamin A (Acetate), Manganese Sulfate, Folic Link, Vitamin D3 (Cholecalciferol), D-Biotin, Vitamin B6, Vitamin K1, Copper Oxide, Chromium Chloride, Vitamin B1, Vitamin B2, Potassium Iodide, Sodium Selenate, Sodium Molybdate, Sodium Metavanadate And Vitamin B12, Packaged Strictly In 100 Tablets In An Original Polyethylene Bottle With A Screw Cap Equipped With A Child Safety System, And A Cardboard Box With Instructions In Kazakh And Russian, With Residual Shelf Life At The Time Of Delivery Of At Least 60% Of The Total Shelf Life, In A Total Quantity Of 20 Packages, Without The Possibility Of Replacement With Analogues Of A Smaller Composition, Multivitamin Generics Without Sodium Metavanadate, Drugs In The Form Of Capsules, Blisters Or With Fewer Tablets In One Package., Magnesium B6, Supply Of A Medicinal Product Registered In The Republic Of Kazakhstan (Atc Code: A12cc30) In The Form Of Oval White Film-Coated Tablets Containing Anhydrous Magnesium Citrate In A Dosage Of 618.43 Mg (Which Is Strictly Equivalent To 100 Mg Of Pure Magnesium) And Pyridoxine Hydrochloride In A Dosage Of 10 Mg As Active Substances, Using Lactose As Excipients Anhydrous, Macrogol 6000 And Magnesium Stearate, Packaged In 20 Tablets In An Original Blister And A Cardboard Box With Instructions In Kazakh And Russian, With A Residual Shelf Life Of At Least 60% At The Time Of Delivery, In A Total Quantity Of 30 Packages., Supply Of A Medicinal Product Registered In The Republic Of Kazakhstan In The Form Of Chewable Tablets With Orange Flavor, Containing A Combination Of Active Substances: Calcium Carbonate 1250 Mg (Equivalent To 500 Mg Of Elemental Calcium) And Colecalciferol 2.0 Mg (Equivalent To 200 Iu Vitamin D3), Packaged In 30 Tablets In High-Density Polyethylene Bottles, In A Total Quantity Of 30 Packages, A Biologically Active Food Supplement (Dietary Supplement) Containing A Concentrate Of Natural Premium Quality Fish Oil In The Form Of Soft Capsules (Gel Capsules), Strictly Original From A Certified International Manufacturer. Content Of Active Substances In One Capsule: Natural Fish Oil Concentrate Of At Least 1000 Mg, Of Which Omega-3 Polyunsaturated Fatty Acids Are At Least 300 Mg, Including Eicosapentaenoic Acid (Epa) At Least 180 Mg And Docosahexaenoic Acid (Dha) At Least 120 Mg. The Capsule Must Be Made From Bovine Gelatin, Glycerin And Water, Without The Use Of Pork Ingredients (Halal/Kosher Friendly). Fish Oil Must Be Molecularly Purified, Distilled, And Tested To Be Free Of Potentially Harmful Levels Of Contaminants (Heavy Metals, Mercury, Pcbs, Dioxins). Release Form: Plastic Bottle With A Sealed Cap Containing Exactly 100 Capsules. Total Purchase Volume: 30 Bottles (Packages). The Product Must Be Registered And Permitted For Use On The Territory Of The Republic Of Kazakhstan, And Have A Certificate Of State Registration (Sgr) Of Dietary Supplements. The Remaining Shelf Life At The Time Of Delivery Must Be At Least 60% Of That Established By The Manufacturer. The Supplier Is Obliged To Provide Documents Confirming The Legal Origin Of The Goods And Distribution Authority., A Drug, A Combined Metabolic Preparation Containing In One Tablet The Active Ingredients: Inosine (Riboxin) Not Less Than 0.25 G, Succinic Acid Not Less Than 0.30 G, Nicotinamide Not Less Than 0.025 G, Riboflavin Sodium Phosphate (Riboflavin) Not Less Than 0.005 G. Release Form: Enteric-Coated Tablets. Pharmacological Group: Other Drugs For The Treatment Of Heart Diseases And Metabolic Agents. The Product Must Be Registered And Approved For Medical Use In The Territory Of The Republic Of Kazakhstan. Total Purchase Volume: 30 Packages. The Drug Must Be Supplied In Original Factory Packaging Containing Labeling In Kazakh And Russian. The Remaining Shelf Life Of The Medicinal Product At The Time Of Delivery Must Be At Least 60% Of That Established By The Manufacturer. The Supplier Is Obliged To Provide A Certificate Of Conformity (Analytical Passport) For Each Batch Of The Drug Upon Delivery.
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