Homeopathic medicines are therapeutically active micro-doses of mineral, botanical and biological substances. They are reliable and safe drugs, therefore considered by many as an excellent first choice when self-medicating. Homeopathy has been used for more than 200 years, building a remarkable safety record and generating a great body of knowledge. Today, homeopathy is used by millions of patients in more than 65 countries and is recommended by more than 400,000 healthcare providers. Since the passing of the federal Food, Drug, and Cosmetic Act in 1938, homeopathic medicines have been regulated as drugs by the United States Food and Drug Administration FDA .1 To be accepted as a homeopathic medicine by the FDA, product ingredients must be identified in the Homeopathic Pharmacopoeia of the United States HPUS or generally accepted as homeopathic under the principles of homeopathy. All Boiron homeopathic medicines are manufactured according to the highest standards, complying with the specifications of the HPUS as well as drug Good Manufacturing Practices GMP. Being regulated as a drug, as opposed to a food or dietary supplement, ensures that homeopathic medicines adhere to drug labeling specifications. Like packaging for conventional over-the-counter drugs, packaging for homeopathic medicines must state specific diseases, ailments, or symptoms for which the product is to be used, the concentration of active substance or substances contained therein, the recommended dosage, and the mode of application. These clear specifications make choices easier for consumers and guidance easier for retailers.