Not only the full ingredients, but full approval by FDA requires that and the continuing study trials updated in real time with the agent that is Brand Named. It is this requirement which then LEGALLY extends the all-important MAJOR difference in these two agents.
Comirnaty, when finally approved for release, will have LIABILITY for product placed on the MANUFACTURER— PFIZER.
The current “hey it’s the same thing” as administered NOW under Emergency Use Authorization- has NO liability whatsoever for Pfizer, and thus NO protection for the public from what is an experimental unapproved agent.
Big Difference. They are attempting to use the EUA as a live trial, and using the fedgov to FORCE injection to drive the trial “participants” (without their INFORMED CONSENT-— which is removed by a signed waiver prior to injection-which the current law and the Nuremburg Laws require in the US).
Good post John Mosby. In addition, the formula of the current Pfizer bioNtech can be changed as often as the manufacturer wants, and disclosure is not required.