EPA is directed by the Federal Insecticide, Fungicide, and Rodenticide Act as amended in 1988 (FIFRA '88) to review all pesticide products containing active ingredients initially registered before November 1, 1984, and to reregister those products that have a substantially complete data base and do not pose unreasonable adverse effect to people or the environment. The pesticide reregistration program is to be completed by the late 1990's. The Reregistration Eligibility Document (or RED) discusses the scientific data and other information supporting EPA's regulatory conclusion that products containing dried blood do not pose unreasonable risks when used as directed by Agency-approved labeling, and are eligible for reregistration.