The content you are trying to access is intended
for healthcare professionals only. 

Are you a healthcare professional?
The content you are about to view is intended for consumers. You are being redirected.
The content you are about to view is intended for healthcare professionals. You are being redirected.


A ready to use emulsion of medium chain triglyceride (MCT) for use in conditions requiring a source of MCT.

Betaquik is suitable from 3 years of age.

Download the betaquik datasheet

Key Features
  • 20% MCT emulsion providing 50g of MCT per 225ml bottle

      o   No added carbohydrate

      o   No added protein

  • Unflavored

      o   Ready to drink

      o   No need to dillute

      o   Can be incorporated into recipes and modular feeds

      o   No oily mouth feel

  • 0.5g LCT per 10g MCT (1g LCT per 100ml / 2.5g LCT per 225ml)

Product Number



Reimbursement Code




15 x 225ml bottles



 WIC-Eligible Medical Food

Advocacy Support and Education Links

The Charlie Foundation: The Charlie Foundation for Ketogenic Therapies was founded in 1994 to provide information about diet therapies for people with epilepsy, other neurological disorders and select cancers.


Matthew’s Friends: The contents of the Matthew’s Friends website has been written by parents, unless otherwise stated. Our aim is to aid and support parents through our own experiences with our children in managing the Ketogenic Diet. We also hope to be able to provide you with the latest information possible with regard to what is going on in the”ketogenic world”.


Epilepsy Foundation: Information, community and resources about epilepsy.


The American Epilepsy Society: The American Epilepsy Society is one of the oldest neurological professional organizations in this country. The Society seeks to promote interdisciplinary communications, scientific investigation and exchange of clinical information about epilepsy.


Glut1 Deficiency Foundation:

The Glut1 Deficiency Foundation is a volunteer, non-profit family organization dedicated to:

  • Educating others about Glut1 Deficiency by creating a forum for sharing support, experiences, resources, and information between patients, families, and healthcare professionals.
  • Increasing awareness of and advocacy for Glut1 Deficiency.
  • Supporting and funding researchers as they work for a cure.


Dravet Syndrome Foundation: Dravet Syndrome Foundation is a volunteer-based, non-profit organization dedicated to aggressively raising research funds for Dravet syndrome, a rare and catastrophic form of epilepsy beginning in childhood, and related conditions. By offering research grants for syndrome-specific research with a novel approach, DSF can move researchers and the medical community forward to find better treatments and a cure while assisting afflicted individuals and their families.

Our product range for disorders of Fat Metabolism 

View product
View product
Inborn Errors of Metabolism