Most vaccines are violating Biologics labeling law
Note: the post calls the product mislabeled or misbranded in a few places. The correct legal term is “misbranded”.
This is Part 2 of my investigation into the fact that most Biologics, including vaccines, non-vaccines, and countermeasures (mRNA shots) are currently in violation of the only statutory labeling requirement for the FDA Biologics licensing (BLA) – listing of the manufacturing facility (not corporate address) on the carton, vial and product insert that comes with it.
In Part 1, I have explained that the main federal law that governs all “biologics” today stems from the 1902 Virus, Serum and Toxin Act in which the Congress required package labels to contain: “the proper name of the article contained therein, the name, address, and license number of the manufacturer, and the date beyond which the contents cannot be expected beyond reasonable doubt to yield their specific results.” Today, this requirement is found in Section 351(a)(1)(B) of the Public Health Service Act (PHS Act), codified at 42 U.S.C. § 262(a)(1)(B). [Source]
The FDA recognized this requirement as mandatory in its 1996 rulemaking in §§ 610.60 and 610.61. There are no exceptions to this statutory requirement: if there are two or more manufacturers involved, all must be listed on the product carton and label. The products held in the Strategic National Stockpile are not exempted.
It is important to note that there are no other strict statutory requirements for biological product labeling! The assessments as to the product contents, safety and efficacy claims are delegated to the FDA, for which the agency has a wide range of discretionary authority.
Review of measles-mumps-rubella (MMR) vaccines distributed in the US.
Measles is alleged to be a viral illness, but causality for the symptoms of rash and fever by “measles virus” has never been established by the scientific method. Thus, it should not be deemed a viral illness at all by anyone scientifically honest (this excludes the government and all their vassals – medical establishment, Big Science, schools, most other professional classes, churches, the courts, etc. – i.e. almost everyone).
Measles is not a viral illness, but instead, it is a preferred fake crisis to enact for every state health board and most governors when they are short on cash or need to push through another civil rights removing law. How often is a crack addicted whore short on cash? It’s a rhetorical question.
Recently, Pennsylvania governor Shapiro tried to fake a measles epidemic by claiming 2 deaths which happened not from measles at all. Bobby Kennedy was immediately game to cosplay the devastation of an unchecked imaginary measles epidemic and started tweeting about sending the CDC hit squad… ahem… “scientists” to “stop the epidemic fast!!!”
I was wondering what the paratroopers from CDC were planning to do – bring hand sanitizer to the badly affected state of Pennsylvania? I think Shapiro lost this time. But he is determined to eliminate the Amish control group at all cost, so this is far from over.
Here is what I found for measles, mumps and rubella (MMRII) shot, which is on CDC “recommended” schedule at 12-15 months of age (causing autism in a significant %), and then at 4-6 years of age, causing additional and more severe autism and many more injuries. MMR shot is on all 50 states school entry requirements, and in several large states it is mandatory, with practically no exemptions.
Before we get to the currently distributed vaccines – as you may know, Trump recently issued Executive Order 14420 which included the following statement:
(b)The Gold Standard Childhood Vaccine Recommendations also recognize that the combined measles, mumps, rubella (MMR) vaccine should be administered in three separate single-disease shots once such products are domestically available and that, to the maximum extent feasible, all childhood immunizations should be administered at separate medical visits.
The most commonly used (since 1971) MMRII vaccine is manufactured by Merck. In response to Trump’s EO, Merck issued a public statement saying that it is not feasible for them to split the product and complete three separate clinical trial programs. I believe them because this is totally crazy based on the economics involved. They won’t do this.
What I also believe – the US government-military-bioweapons cartel masquerading as “vaccine making” will eventually switch all the childhood and other shots to the mRNA platform. This is because the individual government/political actors own large interests in it (Bobby Kennedy’s son RFK III and grandchildren stand to inherit billions from mRNA, Danaher Corp in-laws).
Of course, most MAHA politicians, HHS/DOW/DARPA/BARDA/DTRA/CIA/NSA brass and Trump family already took stakes in all these ventures. It is also cheap and easy to pump out mRNA – no regs, no liability, and it is 100% chemical poison made by chemical reaction, no need to bother with lengthy biologics culturing processes. (Note – biologics culturing doesn’t make anything safe, it’s poisonous for different reasons, but it takes a long time to produce vs 100% chemical mRNA).
Investments into single measles mRNA shots already have been made by Jay Battacharya’s NIH (stay tuned for more reporting on this). Thus, the HHS/DOW/pharma cartel has a plan – shut down the old pharma factories and switch to the new, largely secret manufacturing base. The information about product mislabeling based on the manufacturing facility disclosure is crucial going forward.
While the switch to the government-military-owned mRNA platform is ongoing, turns out, the current Merck’s MMRII vaccine is in violation of the BLA law for product labeling. Hopefully this information will be useful to those trying to fight the unlawful vaccine mandates.
read the rest at sashalatypova.substack.com