Abstract
Growing concern about the spiraling cost of health care in America has increased interest in herbal medications as an alternative to conventional medicine. Due in part to consumer demand for natural alternatives, consumption of herbal medications is increasing in the United States. Because herbal medications are natural, sold without a prescription, and inexpensive, most consumers consider them safe. However, because the Food and Drug Administration ("FDA") prohibits the printing of health-related claims on herbal medication packaging, consumers usually rely on unreliable sources. They consult health food store clerks or outdated and untrustworthy herbal product literature to obtain information regarding side effects, usage, and dosage information.
Recommended Citation
Cataxinos, Edgar R.
(1995)
"Regulation of Herbal Medications
in the United States: Germany
Provides a Model for Reform,"
Utah Law Review: Vol. 1995:
No.
2, Article 12.
Available at:
https://dc.law.utah.edu/ulr/vol1995/iss2/12