Homeopathic drugs in the United States are subject to well-defined regulatory processes that more closely resemble those that apply to allopathic medications than to dietary supplements.
Homeopathic products are under similar regulations as allopathic drugs. Homeopathic products are considered by the FDA as over-the-counter drugs with legal status and can be sold without a doctor's prescription. Homeopathic medicines are prepared and marketed in accordance with FDA Compliance Policy Guide No. 7132.15. Manufacturers of homeopathic medicines are registered with the FDA and licensed by state regulatory agencies. Homeopathic products can legally tell you the benefits and indications of such products.
Remedies are required to meet certain legal standards for strength, quality, purity, and packaging. In 1988, the FDA required that all homeopathic remedies list the indications for their use (i.e., the medical problems to be treated) on the label. The FDA also requires the label to list ingredients, dilutions, and instructions for safe use.
The guidelines for homeopathic remedies are found in an official guide, the Homeopathic Pharmacopoeia of the United States, which is authored by a nongovernmental, nonprofit organization of industry representatives and homeopathic experts.
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