December 2022
UPDATE: FDA Finalizes Homeopathic Guidance

In its final guidance on Homeopathic Drug Products, the FDA intends to prioritize for enforcement and regulatory action specific categories of homeopathic drug products that potentially pose a higher risk to public health such as those intended for populations at greater risk for adverse reactions, as well as ophthalmic and injectable products, because the routes of administration for these products bypass some of the body’s natural defenses.

The agency anticipates many homeopathic drug products will fall outside the categories of drug products it intends to prioritize for enforcement and regulatory action.

While leading homeopathic organizations believe many of the FDA’s assertions, policy choices, legal arguments, and conclusions in the final guidance are incorrect, FDA reiterated that many homeopathic drugs will remain outside of its enforcement priorities.

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“The highest ideal of cure is rapid, gentle and permanent restoration of the health, or removal and annihilation of the disease in its whole extent, in the shortest, most reliable, and most harmless way, on easily comprehensible principles.”
Organon of Medicine, 6th edition
Portrait of Samuel Hahnemann

Dr. Samuel Hahnemann
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