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Prescription Drug Labels

Page history last edited by Skye 8 years, 3 months ago

Prescription Drug Labels


DailyMed: About DailyMed

DailyMed provides access to package inserts and labels for over-the-counter, herbal, and prescription drugs. Labels on DailyMed may not be identical to approved labels nor the labels on currently distributed products. DailyMed is provided by the United States National Library of Medicine. Search by drug name, NDC code, or drug class to locate the package insert.


Drug Information Portal - U.S. National Library of Medicine - Quick Access to Quality Drug Information
This site is a true portal: search for a prescription, over-the-counter, herbal, or nutraceutical name and the site will provide links to additional information from a variety of United States-government-produced websites. Includes links to research articles, drug monographs, labels, and more. Can also be searched by drug category.



Browse or search for United States Food and Drug Administration (FDA) approved prescription and over-the-counter human drugs and therapeutic biologicals currently approved for sale in the United States. The site includes discontinued drugs and "Chemical Type 6" approvals. Contents for each drug include active ingredients; dosage form or route of administration; strength; marketing status; company that sponsored application for approval; FDA action date; and approval type. Many, but not all drug products have links to current FDA approved labels; older labels; approval letters; reviews; and patient information. In addition, new drug applications (NDA) and biologic license applications (BLA) can be listed.


Electronic Medicines Compendium (eMC)
Up to date, easily accessible information about most of the licensed medicines available for use in the United Kingdom (UK). Contains summaries of product characteristics for use by health care professionals as well as patient information leaflets. Maintained by a nonprofit organization funded by UK pharmaceutical companies. Search by drug name or manufacturer name.


Vaccines, Blood & Biologics
The United States Food and Drug Administration (FDA) regulates vaccines, blood products, and biologic products including cellular and gene therapy products as well as tissue transplantation. Information is provided about allergenics, blood and blood products, cellular and gene therapy, tissue and tissue products, vaccines, xenotransplantation (transplantation of non-human cells), international activities, development and approval, compliance and regulation, safety and availability, science and research, news and events, as well as resources for consumers, health professionals, and industry personnel. This is the only FDA database that includes these products (blood, biologics, and vaccines are not included in Drugs@FDA). Search or browse to find regulatory and application information on licensed products and premarket approvals, as well as consumer and professionally-focused information.



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