It's for interpretability, and to have very clear authority to set levels as well. We'll have categories for, perhaps, “prepackaged”. That's a category you see a lot in the regulations. Then, for the levels, we would need regulatory authority to set those. Hypothetically, if it was just for prescribed foods, you could try to build that in, but it's to have the grant of both, because both parameters are going to be very important. Companies will need to know when they are at that level and have it very clearly specified.
For enforceability and clarity, it's good to have both the food and the level.