There is no official approval process or certificate issued from the FDA to approve the sale of food or juice products in the United States. The Food and Drug Administration, however, has established stringent laws and regulations, called Good Manufacturing Practices (GMPs) to ensure the safety of foods manufactured and sold in the U.S. MonaVie is manufactured in a GMP compliant facility.

The U. S. Congress passed the Dietary Supplement Health and Education Act (DSHEA) of 1994 which spells out the regulations as they apply to dietary supplements. See similar questions...

Quit For Sure products are 100% all-natural herbal solutions to help you quit smoking. According to Food and Drug Administration guidelines, Quit For Sure products are classified as nutritional supplements. Our products are not intended to diagnose, treat, cure, or prevent any disease. These statements have not been evaluated by the FDA. See similar questions...

The FDA only approves substances considered to be drugs, not foods. Therefore, FDA approval process is not relevant to Whole-istic Solutions' all-natural products. Nevertheless, every Whole-istic Solutions product is in full compliance with all applicable FDA regulations and all ingredients in Whole-istic Solutions products are in the FDA’s GRAS (Generally Regarded As Safe) category. See similar questions...

The FDA does not grant approval to Nutraceuticals, only prescription drugs. We are, however, regularly inspected by the FDA and the Texas Department of Health and must adhere to the highest of standards of Good Manufacturing Practices including laboratory analysis and product testing for potency and purity. See similar questions...

The Food & Drug Administration does not have an approval process for any nutritional supplements, only perscription medications. However, Flexcin is manufactured in a FDA inspected and approved facility. See similar questions...

The price of the test is $200, including shipping costs. Payment can be made by any major credit card by the individual or by the ordering physician or clinic, by including the card details on the test request form. Samples submitted anonymously must be accompanied by a valid credit card number from the respective doctor or affiliated health care institution. See similar questions...

Currently, non-prescription nutritional supplements do not require FDA approval. However, BioVitale's Digestive Enzyme Complex is manufactured in a FDA monitored and approved facility under the highest quality control standards. See similar questions...

The anti-pathogenic and germicidal properties of the silver oxide in Safe Lips has been tested by 14 reputable and independent Contract Research Organizations (CROs). Countless individuals have contacted us with their very positive feedback, declaring the Safe Lips was the major factor in returning them to healthy skin. Furthermore, we have a very liberal return policy where customer satisfaction is 100% guaranteed, and yet we have experienced very few returns. See similar questions...

Yes, most of our users of the Quit Smoking Support System reported that they managed to stop smoking and no longer experienced cravings or withdrawal symptoms. Few smoking cessation products out there can make such similar claims in efficacy, ease, and successfulness. See similar questions...

ECP is approved by the FDA for the treatment of Angina and Congestive Heart Failure. It has undergone rigorous clinical trials at leading universities around the country and ECP has been the subject of scientific studies published in leading medical journals. See similar questions...

The US Food and Drug Administration (FDA) does not approve or disapprove of any kind of dietary supplements, such as Revivol ™, since it is not within their responsibility. The FDA only approves or disapproves of pharmaceutical drugs, which Revivol™ is not. See similar questions...

ZymaDerm is 'FDA Compliant' and conforms to the standards of the Homeopathic Pharacopeia of the United States (HPUS), a compendium recognized as both official and authoritative by the FDA. Each of the ingredients in ZymaDerm is stated in the Pharmacopeia to be useful as an aid in the treatment of skin rash conditions. If a drug-free agent is listed in the HPUS for treating certain conditions, a product containing that agent may be marketed for those conditions without specific FDA approval. See similar questions...

Our entire service has been scientifically reviewed for safety and effectiveness by the U.S. Food and Drug Administration (FDA). FDA granted Home Access Health nationwide clearance to market its service on April 28, 1999. The Home Access at-home telemedicine Hepatitis C counseling and testing service is the ONLY such service available in the United States approved by the U.S. Food and Drug Administration. See similar questions...