Fluoride – The Only Drug Intentionally Added to Your Tap Water

Michael Connett, JD

Following the recent water crisis in Flint, it’s no wonder that the U.S. public has begun to question exactly how safe our drinking water actually is. What was once taken for granted — the idea of safe, pure, and drinkable water for everyone — is now in serious question.

In addition to the continuing problems with lead contamination, it has come to light in recent years that public water supplies are now contaminated with trace levels of pharmaceutical drugs, including oral contraceptives and mood stabilizers.

These drugs end up in our water somewhat inadvertently; however, there’s one pharmaceutical that is intentionally added to our tap water: Fluoride.

Fluoride Is a Neurotoxic, Endocrine-Disrupting Drug

Fluoride is an endocrine-disrupting, neurotoxic, and bone-weakening substance that the Food and Drug Administration (FDA)defines as a drug when used to prevent disease, because unlike the minerals we need (e.g. calcium), humans have no known physiological requirement for fluoride.

Sodium fluoride, long known as an effective roach poison, is added to tablets and drops (i.e., “fluoride supplements“) for the purpose of preventing tooth decay. But because of fluoride’s toxicity, you cannot purchase fluoride “supplements” over-the-counter; they can only be dispensed by prescription under the supervision of a doctor. In short, sodium fluoride is not a nutritional “supplement;” it is a prescription drug, and a dangerous one.

Although fluoride drugs have been prescribed for over 50 years, the FDA recently announced that marketing fluoride drops and tablets for cavity prevention violates federal law, because FDA has never approved these products as either safe or effective.

FDA made this stunning declaration in a Warning Letter, in which the Agency called on a manufacturer to immediately cease selling fluoride drops and tablets. Removing harmful fluoride drugs from the market will protect the health of millions of children, but we also need to address the big elephant in the room: water fluoridation.

With water fluoridation, cities and towns can add almost the same dose of fluoride contained in prescription fluoride drops and tablets to each glass a toddler drinks — with no supervision of a health professional, and without the informed consent of the patient.

FDA Issues Warning Letter

On January 13, 2016, the FDA sent a “Warning Letter” to Kirkman Laboratories, Inc., demanding that the manufacturer immediately discontinue the marketing of its fluoride drops and tablets.

The FDA’s Warning Letter clearly states that fluoride drops and tablets are “unapproved new drugs” because: (1) they are not generally recognized as safe and effective for caries prevention purposes, and (2) no manufacturer has ever provided FDA with adequate studies to demonstrate the drugs’ safety and effectiveness.

This isn’t the first time FDA has stated that fluoride drops and tablets are unapproved drugs; FDA first grudgingly admittedthis bewildering fact in the 1990s in response to a dogged investigation by the late New Jersey Assemblyman John Kelly.

What makes the Warning Letter to Kirkman so significant, however, is that the FDA has finally decided to take enforcement action against a company producing these drugs.

FDA’s Warning Letter is a historic development, but much remains to be done. The real test will be whether FDA follows through on its own conclusions by going after the larger companies that are currently manufacturing the very same fluoride drugs.

Three of the largest companies making fluoride drops/tablets today are Libertas Pharma Inc., Sancilio & Company, Inc., and Qualitest and so far, FDA has not taken any action against these companies.

For this reason, the Fluoride Action Network (FAN) and International Academy of Oral Medicine & Toxicology (IAOMT) have filed a Citizens Petition with the FDA that calls upon the agency to take enforcement action against all companies, not just Kirkman, that continue to produce unapproved fluoride drugs. The petition asks that these unsafe and ineffective drugs be removed from the market entirely. To support the FAN/IAOMT petition, please sign this online letter to FDA.

Pharmacies Are Violating Federal and State Law

It’s not just the fluoride drug manufacturers who are violating the law. The nation’s largest pharmacies are culprits as well. FAN recently conducted an undercover investigation of the nation’s four largest pharmacies: Walgreens, CVS, Rite Aid, and Walmart.

Read More HERE

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