Download Cosmetic regulation in a competitive environment by Norman F. Estrin, James M. Akerson PDF

By Norman F. Estrin, James M. Akerson

ISBN-10: 0824775163

ISBN-13: 9780824775162

A precis of present and rising family and foreign regulatory concerns. It delineates the jobs of businesses and programmes to navigate the legislative mass - for giant and small own care businesses. The participants describe the commonest technique of accomplishing security exams to guage inflammation, sensitization, photoirritation and photosensitization.

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Extra info for Cosmetic regulation in a competitive environment

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Implementation of the 1938 Act Shortly after enactment of the 1938 Act, FDA met with food, drug, and cosmetic manufacturers and with the coal tar color manufacturers to make plans for implementation of the new color additive provisions [69]. Although the industry initially stated that there were some 1,500 color additives used in drugs and cosmetics, this was soon reduced to about 300 substances [69]. During the conferences, this list of 300 substances was further reduced on the basis of toxicity, extent of use, essentiality, duplication, stability, and chemical purity [69, 70].

Feeding studies on FD&C Red No. 4 sponsored by the Pharmaceutical Manufacturers Association (PMA) had produced a number of bladder lesions in the test animals. The PMA concluded that the lesions were related solely to catheterization of the test animals during testing, not to the test color additive. Nonetheless, FDA delisted the color additive for ingested uses in September 1976 [130] while at the same time permanently listing it for cosmetic and external drug use [131]. This had a major impact on the producers of maraschino cherries, for whom the continued availability of FD&C Red No.

The conclusion of this review was that: “No one at this time can tell how much or how little of a carcinogen would be required to produce cancer in any human being, or how long it would take the cancer to develop” [101]. After introducing the entire report into the record of the hearing on the bill, the Secretary testified as follows: This is why we have no hesitancy in advocating the inclusion of the anticancer clause. Unless and until there is a sound scientific basis for the establishment of tolerances for carcinogens, I believe the Government has a duty to make clear—in law as well as in administrative policy—that it will do everything possible to put persons in a position where they will not unnecessarily be adding residues of carcinogens to their diet [101].

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Cosmetic regulation in a competitive environment by Norman F. Estrin, James M. Akerson


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