Daniel Fabricant (Tag Archives)
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NMN, FDA, and the Supplement Industry’s Fight for Its Life (Updated 3/29/23)
Background: A battle is brewing between the dietary supplement industry and the FDA. It’s over the legal status of an ingredient known as NMN, a natural vitamin with powerful anti-aging potential. After a company followed the guidelines to get[…] Continue Reading →
FDA Announcement on CBD: We Need Help from Congress
On January 26th, 2023, the FDA made a major announcement regarding CBD (Cannabidiol), coming after years of deliberation, debate, and discussion. The gist of the message:
“We need help from Congress!”
View this post on Instagram2022 Supplement Industry Awards | PPP #079
It’s that time of year again — time for PricePlow’s 2022 Supplement Industry Awards. Mike and Ben sat down to review 2022, and then got into a batch of awards similar to what we did in the 2021 Supplement […] Continue Reading →
The NPA is Fighting Dick Durbin’s 2022 Supplement Bill (S.4090) | PPP #067
https://blog.priceplow.com/podcast/npa-vs-dick-durbin-s4090
On April 26, Senators Dick Durbin (IL) and Mike Braun (IN) proposed a bill titled Dietary Supplement Listing Act of 2022,[1,2] which would have serious ramifications on the way business and commerce is done in the dietary supplement […] Continue Reading →
Mahmoud ElSohly & Ikhlas Khan’s $2.3 Million FDA Tax Waste: Incomplete Results Published
This is part four of a six page series researching whether DMAA (1,3 dimethylamylamine) is a natural constituent of geranium flowers. All six parts are linked from our main DMAA in Nature / Geranium page.
Given the rancid stench […] Continue Reading →
The Ten (Actually 11!) Times DMAA was Found in Nature (in Geraniums)
One of the most pivotal parts of the DMAA Lawsuit between Hi-Tech Pharmaceuticals and the FDA is whether or not DMAA is found in nature. Specifically, is the stimulant (also known as 1,3 dimethylamylamine) a natural constituent of certain […] Continue Reading →
The 2016 FDA NDI Draft Guidance Document: How To Destroy The ENTIRE Dietary Supplement Industry in 102 Pages
Disclaimer: This article was co-authored by Bruce Kneller and Mike.
On August 12th 2016, the FDA published a new Draft Guidance Document for NDIs (New Dietary Ingredients), in the Federal Register. Since this document is 102 pages long, there […] Continue Reading →
Eric Schneiderman’s Supplement Lab Tests: The REAL False Claims?
Update, May 8, 2018: The Attorney General behind this fiasco, Eric Schneiderman, has resigned after at least four accusations of extremely racist sexual abuse. Even crazier, his criminality was predicted by President Trump as far back as 2013.[Tweet[…] Continue Reading →
