Word: toed
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Dates: during 1960-1969
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The first U.S. Pure Food and Drug Law, passed in 1906, gave, the enforcement authority (now the Food and Drug Administration) no power to rule on the safety of any substance that a food processor proposed to put in his packages. Not until 1958 did Congress give the FDA the...
The FDA's list of GRAS items classifies hundreds of additives by their principal purposes. Among them are anti-caking agents, which keep such things as salt, sugar and milk powder from clumping; preservatives (31 listed); emulsifying agents, used to help homogenize substances that do not normally mix (like...
In all, there are thousands of permitted additives, and few have ever been tested thoroughly for possible long-term harmful effects in man. No one can be really certain that any particular substance may not induce cancer over a 50-year period, or cause thalidomide-like deformities in the unborn...
Saccharin has been known since 1879, and widely used since the early 1900s. Entirely synthetic and unknown in nature, saccharin provides no calories and nothing to elevate the diabetic's blood sugar. Its one drawback is that in many users' mouths it leaves a bitter, aftertaste. The cyclamates...
Crude Guillotine. Cyclamates, given in doses 50 times greater than any likely human consumption, have caused bladder cancer in mice and rats, as well as the birth of deformed chicks. This was duly reported to the FDA by Abbott Laboratories, major producer of cyclamates. Within a week, Secretary Robert Finch...