DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Part 172 [Docket No. 91F-0228] Food Additives Permitted For Direct Addition to Food For Human Consumption; Sucrose Acetate Isobutyrate

DEPARTMENT OF HEALTH AND HUMAN SERVICES FOOD AND DRUG ADMINISTRATION [Docket No. 75F-03551 ASPARTAME DECISION OF THE PUBLIC BOARD OF INQUIRY

DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Parts 315 and 601

The Food and Drug Administration (FDA) is reopening until February 12, 1999, the comment period for the draft guidance for industry entitled ‘‘Draft Guidance for Industry on Developing Medical Imaging Drugs and Biologics’’ that appeared in the Federal Register of October 14, 1998 (63 FR 55067). FDA is taking this action in response to a request for an extension. DATES: Written comments on the d...

BILLING CODE 4160–01–F DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration

period of 5 years. Any person with an approved or pending drug product application who knowingly uses the services of Mr. Feuer in any in any capacity during his period of debarment will be subject to civil money penalties (section 307(a)(6) of the act (21 U.S.C. 335b(a)(6))). If Mr. Feuer, during his period of debarment, provides services in any capacity to a person with an approved or pending...

Hygienic Quality of Meat Products in Qazvin Province during (2011-2014), Iran

Background & Aims of the Study: One way to increasing shelf life of meat is the production of sausages along with additives. One of these additives contains nitrite that in an acceptance limit is not a threat for human health but if it's amount is higher than standard, it will react in the body with secondary amine and the result is the formation of...

Department of Health and Human Services Food and Drug Administration 21 Cfr Part 101 Food Labeling: Health Claims and Label Statements; Folic Acid and Neural Tube Defects

Agency: Food and Drug Administration, HHS. Action: Final Rule. __________________________ SUMMARY: The Food and Drug Administration (FDA) is announcing its decision not to authorize a health claim for folic acid and neural tube defects at this time. However, consistent with the recently announced recommendations of the U.S. Public Health Service (PHS) that all women of childbearing age in the U...