Medications Available Without a Prescription

by Food and Drug Administration (FDA)

For those who yearn to break their cigarette addiction but don't fancy a trip to the doctor's office, the ability to get the nicotine patch without a physician's prescription may be just what the doctor ordered.

Until less than a year ago, the nicotine patch was available by prescription (Rx) only. In July 1996, the Food and Drug Administration approved the "switch" of the Nicotrol patch to over-the-counter (OTC) status, following on the heels of a February 1996 switch of another stop-smoking aid containing nicotine, Nicorette gum. Then, on Aug. 2, FDA approved the switch of a second nicotine patch, Nicoderm CQ.

The patch and gum join more than 600 other OTC drugs that, according to the Nonprescription Drug Manufacturers Association, would have required a prescription only 20 years ago. The 600-plus products are now available without a prescription because FDA, in cooperation with panels of outside experts, determined they could be used safely and effectively without a doctor's supervision.

In the last year and a half alone, FDA has given OTC approval to drugs with such household names as Children's Advil and Children's Motrin (ibuprofen), Orudis KT (ketoprofen) and Actron (naproxen sodium), for pain relief and fever reduction; Femstat 3 (butoconazole nitrate) for vaginal yeast infection; Pepcid AC (famotidine), Tagamet HB (cimetidine), Zantac 75 (ranitidine hydrochloride), and Axid AR (nizatidine), for heartburn; and Rogaine (minoxidil) for hair growth.

Over-the-counter switches provide increased access to effective drugs. Eighty-five percent of Americans feel it is important to have OTC medications available to relieve minor medical problems, according to a 1992 Heller Research Group study of "Self Medication in the '90s: Practices and Perceptions."

"There is an important trend toward consumer participation in their own health care," says Debra Bowen, M.D., director of FDA's division of over-the-counter drug products. "It's part of our mission to keep up with the consumers' wish to be more involved."

Switches have a huge impact on the health-care economy. The greater availability of medicines over the counter saves approximately $20 billion each year, according to the 1995 Physicians' Desk Reference for Nonprescription Drugs, a book of drug information published annually by Medical Economics in cooperation with drug manufacturers. The $20 billion takes into account prescription costs, doctor visits, lost time from work, insurance costs, and travel.

The Switch Process

The original Federal Food, Drug, and Cosmetic Act of 1938 made no clear-cut distinction between Rx and OTC drugs. The 1951 Durham-Humphrey amendments to the act set up specific standards for classification.

The amendment requires that drugs that cannot be used safely without professional supervision be dispensed only by prescription. Such drugs may be deemed unsafe for nonprescription use because they are habit-forming or toxic, have too great a potential for harmful effects, or are for medical conditions that can't be readily self-diagnosed.

All other drugs can be sold OTC. A drug must be made available without a prescription if, by following the labeling, consumers can use it safely and effectively without professional guidance.

Some drugs are approved initially as OTC drugs. More often, though, medications are first approved Rx and later switched. "While a product is available by prescription, we can learn about the drug's safety profile in a much more controlled environment," Bowen says.

Drugs are commonly switched one of two ways: under the "OTC drug review," or by a manufacturer's submission of additional information to the original drug application.

The OTC drug review is an ongoing assessment by panels of nongovernment experts of the effectiveness of all drugs approved before 1962, before proof of efficacy was a requirement. The panels also review prescription ingredients to determine if some are appropriate for OTC marketing. About 40 former prescription-only drug ingredients have been switched by this process.

The second common path to OTC approval is submission of data to FDA (almost always by a manufacturer) showing the drug is appropriate for self-administration. Often the submission includes studies showing that the product's labeling can be read, understood and followed by the consumer without the guidance of a health-care provider. FDA reviews the new data, along with any information known about the drug from its prescription use.

In almost every case, the agency has sought the recommendation of a joint advisory committee made up of members of the agency's Nonprescription Drugs Advisory Committee and another advisory committee with expertise in the type of drug being considered. For example, because Rogaine is for conditions of the hair and scalp, representatives of the Dermatologic and Ophthalmic Drugs Advisory Committee participated.

While not bound by the advisory committee's counsel, FDA almost always follows its recommendation.

About the Author

www.fda.gov
FDA is A United States government body that oversees medical devices, including contact lenses, intraocular lenses, excimer lasers and eyedrops. In the US, these products must be approved by the FDA before they can be marketed.