Absonutrix Gets Its Second FDA Warning Letter In Two Years

For the second time in just over 2 years the U.S. Food and Drug Administration, or FDA, has made public a formal warning letter to supplement company Absonutrix and its owner, Himanshu Nautiyal.

From the letter, which is dated August 26, 2019, we learn that FDA inspectors paid a visit to the company's manufacturing facility back in March. While there, they reportedly collected labels of various products.

As a result of that inspection Absonutrix stands accused of what the agency refers to as "serious violations" of the Federal Food, Drug and Cosmetic Act. And those alleged violations cause some of the company supplements to be deemed "adulterated" or "misbranded".

The letter is redacted in places so it's hard to know exactly how "misbranded" Absonutrix's products are but at least 3 of them allegedly contain less of their dietary ingredient than their labels claim. Those products are:

Absonutrix Uridine 500 mgAbsonutrix NAD Power Boos…

Mero Macho Recall - Drug Tampering Found

Mercury Poisoning From Face Cream

Instant Pot Recall - The TRUTH Behind The Social Media Hysteria

Privacy International Accuses Period-Tracking Apps Of Sharing Intimate Info

FDA: "Avoid THC Vaping Liquids"

Coffee, Tea & Water - FREE eBook

Octonauts - Marine Science For Very Young Children

Black Lemonade - What Is It? Does It Work?

Peep and the Big Wide World - Science For Very Young Children

Did A Himalayan Salt Lamp Really Poison A Cat?

Is There Really A Best Way To Make Coffee?

How To Make Oatmeal In Your Instant Pot