Zhong Nong Yuan Fang Holdings Inc (ANAS)

[JJAAMMAANN]

$$$ ANAS $$$ All Natural Supplement Money Maker!

So long as Alternaturals markets their products as All Natural supplements and does not put in any new ingredients that have not been pre-approved as "Dietary Ingredients", they DO NOT NEED FDA APPROVAL". The FDA can monitor their processes in manufacturing, but seeing how Kush Creams will be doing the manufacturing, it is Kush Creams who has to meet the FDA requirements for CGMP(Current Good Manufacturing Practices). They only have to be registered under the Bioterrorism Act with FDA before producing or selling supplements... Since they are in the buisness of Manufacturing and Selling for a couple years now...Guess is that they are already registered, or they would have been shut down a long time ago.

The PR released by ANAS stated that they wanted to get it to shelves in Colorado around June 30th...This new process is for Washington State where there are new "State" regulations for prepared products and food products.

It may be delayed a few months in Washington State because that is where Kush Creams is located at, and they have to follow the Laws of the State. Again, a good thing because 5 Hour High and our affiliation with Kush Creams is going to be Huge for the future of this company!

Look for more updates soon regarding Financial Projections and sales thus far...along with updates on Share Buy Back, and this baby is going to Soar!

What is FDA's role in regulating dietary supplements versus the manufacturer's responsibility for marketing them?

In October 1994, the Dietary Supplement Health and Education Act (DSHEA) was signed into law by President Clinton. Before this time, dietary supplements were subject to the same regulatory requirements as were other foods. This new law, which amended the Federal Food, Drug, and Cosmetic Act, created a new regulatory framework for the safety and labeling of dietary supplements.Under DSHEA, a firm is responsible for determining that the dietary supplements it manufactures or distributes are safe and that any representations or claims made about them are substantiated by adequate evidence to show that they are not false or misleading. This means that dietary supplements do not need approval from FDA before they are marketed. Except in the case of a new dietary ingredient, where pre-market review for safety data and other information is required by law, a firm does not have to provide FDA with the evidence it relies on to substantiate safety or effectiveness before or after it markets its products.Also, manufacturers need to register themselves pursuant to the Bioterrorism Act with FDA before producing or selling supplements. In June, 2007, FDA published comprehensive regulations for Current Good Manufacturing Practices for those who manufacture, package or hold dietary supplement products. These regulations focus on practices that ensure the identity, purity, quality, strength and composition of dietary supplements.

http://www.fda.gov/food/dietarysupplements/qadietarysupplements/#FDA_role

In My Personal Opinion Of Course!
Long ANAS!