MEDICAL NUTRITION PRODUCTS
PKU Start
Powdered protein substitute for the dietary management of Phenylketonuria from birth.
PKU Trio
Powdered protein substitute for use in the dietary management of Phenylketonuria from 1 year of age.
PKU Gel
Powdered protein substitute for the dietary management of Phenylketonuria. Unflavoured PKU gel is suitable from 6 months to 10 years of age. Flavoured PKU gel is suitable from 1 to 10 years of age.
PKU Express
Powdered protein substitute for the dietary management of Phenylketonuria from 3 years onwards.
PKU Cooler 10,15 y 20
Ready-to-drink protein substitute for the dietary management of Phenylketonuria from 3 years onwards.
PKU Air
Ready-to-drink protein substitute for the dietary management of Phenylketonuria from 3 years onwards.
PKU Sphere
Powdered protein substitute containing GMP for the dietary management of Phenylketonuria from 4 years of age onwards.
Tyrosine
A powdered tyrosine amino acid supplement for the dietary management of inborn errors of metabolism from 3 years of age onwards.
Flavourpac
A range of powdered, protein free flavour sachets for use with unflavoured protein substitutes. Suitable from 3 years of age and available in: blackcurrant, orange, raspberry and tropical flavours.
Vitabite
A low protein, high energy chocolate flavored bar for use in the dietary management of children from 1 year of age and adults on protein restricted diets.
MSUD Gel
Powdered protein substitute for the dietary management of Maple Syrup Urine Disease from 6 months to 10 years of age.
MSUD Express
Powdered protein substitute for the dietary management of Maple Syrup Urine Disease from 3 years onwards.
Isoleucine
A powdered isoleucine amino acid supplement for the dietary management of inborn errors of metabolism from birth.
Valine
A powdered valine amino acid supplement for the dietary management of inborn errors of metabolism from birth.
MMA/PA Gel
Powdered protein substitute for the dietary management of Methylmalonic Acidaemia and Propionic Acidaemia from 6 months to 10 years of age.
GA Gel
Powdered protein substitute for the dietary management of Glutaric Aciduria type 1 from 6 months to 10 years of age.
HCU Gel
Powdered protein substitute for the dietary management of Homocystinuria from 6 months to 10 years of age.
HCU Express
Powdered protein substitute for the dietary management of Homocystinuria from 3 years onwards.
Cystine
A powdered cystine amino acid supplement for the dietary management of inborn errors of metabolism from 3 years of age onwards.
TYR Gel
Powdered protein substitute for the dietary management of Tyrosinaemia from 6 months to 10 years of age.
TYR Express
Powdered protein substitute for the dietary management of Tyrosinaemia from 3 years onwards.
TYR Cooler 10, 15 y 20
Ready-to-drink protein substitute for the dietary management of Tyrosinemia from 3 years onwards.
TYR Sphere
Powdered protein substitute containing GMP for the dietary management of Tyrosinemia from 3 years of age onwards.
UCD Trio
Powdered protein substitute for the dietary management of Urea Cycle Disorders from 1 year of age.
EAA Supplement
Powdered protein substitute for the dietary management of Urea Cycle Disorders from 3 years of age onwards.
Arginine
A powdered arginine amino acid supplement for the dietary management of inborn errors of metabolism from birth.
Docomega
Powdered docosahexaenoic acid (DHA) for the dietary management of inborn errors of metabolism. Suitable from birth.
Glycosade
a long acting starch, which may help increase the time between meals/snacks. For the dietary management of Hepatic Glycogen Storage Disease. Unflavoured is suitable from 2 years of age onwards
Lipistart
A nutritionally complete powdered formula for the dietary management of long‐chain fatty acid oxidation disorders, fat malabsorption and disorders requiring a high medium‐chain triglycerides (MCT) and low long‐chain triglycerides (LCT) diet. Lipistart is suitable from birth to 10 years of age.
MCT Procal
A neutral‐tasting food fortifier and medium‐chain triglyceride (MCT) supplement. For use in the dietary management of fat malabsorption and other disorders requiring a high MCT, low long‐chain triglyceride (LCT) supplement. MCTprocal is suitable from 3 years of age.
K.Quik
A ready to use, palatable emulsion of medium‐chain triglycerides (MCT) for use in conditions requiring a source of MCT. K.Quik is suitable from 3 years of age.
K.Yo
A unique, ready to eat, palatable semi-solid food for use in the ketogenic diet. Suitable from 3 years of age onwards.
K.Quik
A ready to use, palatable emulsion of medium‐chain triglycerides (MCT) for use in conditions requiring a source of MCT. K.Quik is suitable from 3 years of age.