Food Additives: Competitive, Regulatory, and Safety Problems : Hearings Before the Select Committee on Small Business, United States Senate, Ninety-fifth Congress, First Session ... January 13 and 14, 1977, Part 1U.S. Government Printing Office, 1977 - 979 pages |
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Common terms and phrases
ACETATE acetylsalicylic acid allergic-type Allergy Amendment angioedema animals approved aspartame aspirin intolerance aspirin-sensitive patients bladder bronchial asthma bronchospasm CALCIUM cancer Capsules carcinogens CARRAGEENAN charin chemicals chloride chronic Clinical color additives Commissioner compounds CONGRESS containing FD&C Yellow Cosmetic Act D&C Red Delaney Clause diet dose Drug Administration drug product erythrosine evaluation Externally applied FD&C Yellow FDA's FEDERAL REGISTER FEMA FFMA FIMA final regulation Flavor food additives Food and Drug food colors GLYCOL GRAS 24 Health human ingested intolerance to aspirin labeling Laboratories levels manufacturers METHYL mutagenic nasal NOTE 4A OTC drugs percent Pharmaceuticals PHOSPHATE POTASSIUM proposed provisionally listed Pulvules rats reactions recognized as safe rhinitis risk saccharin safety salicylate SALT Samter scientific Senator NELSON sensitivity Settipane SODIUM studies substances Sufficient for purpose sweeteners symptoms Tablets tartrazine TECHNICAL EFFECTS tion toxicity toxicological tumors urticaria
Popular passages
Page 559 - That no additive shall be deemed to be safe if it is found to induce cancer when ingested by man or animal, or if it is found, after tests which are appropriate for the evaluation of the safety of food additives, to induce cancer in man or animal...
Page 447 - ... generally recognized, among experts qualified by scientific training and experience to evaluate its safety, as having been adequately shown through scientific procedures (or, in the case of a substance used in food prior to January 1, 1958, through either scientific procedures or experience based on common use in food) to be safe under the conditions of its intended use...
Page 408 - Formulary, or any supplement to any of them ; and (2) articles intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease in man or other animals; and (3) articles (other than food) intended to affect the structure or any function of the body of man or other animals...
Page 428 - Operations not later than 60 days after the date of the report, and to the House and Senate Committees on Appropriations with the agency's first request for appropriations made more than 60 days after the date of the report.
Page 40 - ... a full description of the methods used in, and the facilities and controls used for, the production of such additive.
Page 561 - Secretary shall take into account the extent to which the use of such substance is required or cannot be avoided in the production of each such article, and the other ways in which the consumer may be affected by the same or other poisonous or deleterious substances.
Page 61 - I will be happy to answer any questions you and other members of the committee may have.
Page 46 - food additive" means any substance the intended use of which results or may reasonably be expected to result, directly or indirectly, in its becoming a component or otherwise affecting the characteristics of any food...
Page 408 - new drug" means — (1) Any drug (except a new animal drug or an animal feed bearing or containing a new animal drug) the composition of which is such that such drug is not generally recognized, among experts qualified by scientific training and experience to evaluate the safety and effectiveness of drugs, as safe and effective for use under the conditions prescribed, recommended, or suggested in the labeling thereof, except that such a drug not so recognized shall not be deemed to be a "new drug...
Page 453 - ... (ii) the cumulative effect, if any, of such additive in the diet of man or animals, taking into account the same or any chemically or pharmacologically related substance or substances in such diet...