Certificate number:RU.77.99.88.003.Е.002226.02.15
Date of registration and renewal:04.02.2015
Dosage form: & nbspTablets weighing 500 mg.
Classification "Composition" & nbsp BAD - products of plant, animal or mineral origin
Composition: & nbspLactulose is dry, Jerusalem artichoke powder, hyaluronic acid, calcium stearate.
Scope: & nbspFor sale to the population through the pharmacy network and specialized stores, departments of the trade network as a biologically active food additive - a source of lactulose, inulin, hyaluronic acid.
Suggested Usage: & nbspAdults take 2 tablets 3 times a day with meals. Duration of admission is 14 days.
Contraindications:Individual intolerance to the components of the product, pregnant and lactating women.
Special instructions:Before use, it is recommended to consult a doctor.
Shelf life:2 years.
Storage conditions:Store in a dry place, protected from light, out of reach of children, at a temperature not exceeding + 20 ° С.
Research protocols:In exchange for the certificate of state registration No.RU.77.99.11.003.Е.040087.09.11 dated 23.09.2011, the expert opinion of the Federal State Unitary Enterprise ФЦЗ ФЦГ and Э Роспотребнадзора №10-2 ФЦ / 6144 from 09.12.2008, the test report of the FGBU "Tula Interregional Veterinary Laboratory "ROSSELHOZNADZORA №17235 dated 11/28/2014.
Recipient:NPP Tula industry LTD, Open CompanyNPP Tula industry LTD, Open Company Russian Federation
Information update date: & nbsp22.03.2017
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