Randomised, controlled, open label, cross-over trial to evaluate the tolerance of a new paediatric sip feed in children in need of oral nutritional support.

1. Male and female subjects, aged 3-12 years (including 3 and 12 years) in need of oral nutritional support (subject can be current or new paediatric sip feed user);

2. Subject requires a paediatric sip feed for at least 6 weeks;

3. Both hospitalized subjects and out-patients;

4. Stable health status and expected to remain stable throughout the study (in the opinion of the Health Care Professional);

5. Written informed consent from parents/guardian and subject (if applicable according to local law).

1. Cow’s milk allergy, known inflammatory bowel diseases, bowel resection;

2. Subjects requiring a fibre-free diet;

3. Known allergy for fruit (apple, pear, strawberry, raspberry, banana, apricot, lemon) and/or carrot;

4. Subjects requiring an adult rather than a paediatric sip feed;

5. Major renal dysfunction (if requiring, but not yet receiving, dialysis);

6. Major hepatic dysfunction (e.g. hepatitis, congenital abnormalities affecting the liver);

7. Major gastrointestinal intolerance (e.g. vomiting, diarrhoea);

8. Inherited metabolic disorders, including galactosaemia;

9. Use of parenteral feeding and/or enteral tube-feeding;

10. Investigator's uncertainty about the willingness or ability of the child/carer to comply with the protocol requirements;

11. Participation in any other study involving investigational or marketed products concomitantly or within two weeks prior to entry into the study.