Because i.Doc produces PDFs , the preferred FDA format, and automates and standardizes the process it can save time and money in the preparation of FDA compliant submissions.

Yes. All anti-fungals intended for use on humans are regulated by the FDA and must follow their exact guide lines. The 1% active ingredient, Tolnaftate is the maximum % allowed by the FDA. You can't buy a stronger formula, without a prescription.

Yes! Regardless of your health challenge (diabetes, obesity, etc.), you need to first detoxify your whole body and this is what the FBD does ? detoxify the whole body from head to toe. You can always perform the Diabetic or Weight Loss regimen after detoxing to key in on a particular health challenge or pathology.

A.- With billions of dollars spent each year in research with additional billions taken in from the cancer-related sale of drugs, and with vote-hungry politicians promising ever-increasing government programs, we find that, today there are far more people making a living from cancer than are dying from it. A.- NO.

The FDA does not approve any dietary supplements. They only approve drug products. The FDA has a list of guidelines and ingredients commonly referred to as the GRAS List (Generally Recognized as Safe). Ingredients on this list are considered to be pre-approved. All the ingredients in Seasilver are on this list or fall into their pre-approved guidelines.

The FDA issued a public health advisory concerning the use of Vioxx. This advisory is not a recall and is based on Merck & Co.'s voluntary withdrawl of Vioxx from the market due to safety concerns.

A health claim is a very powerful message. In the history of the FDA there have been only 10 approved health claims. A health claim is the association of a food or substance with a direct connection to a disease or a medical condition. In October 2000, the FDA approved the health claim: soy protein in conjunction with a diet low in saturated fat and cholesterol may reduce the risk of heart disease by decreasing serum cholesterol levels.

The product is regulated like all food supplements by the Food and Drug Administration (FDA). The pine cones from which the botanical compound is extracted are considered GRAS (Generally Recognized as Safe) by the FDA as a food and food supplement ingredient. We follow the regulations of the Dietary Supplement Health Education Act of 1994 (DSHEA).

The FDA does not approve any dietary supplements. They only approve drug products. The FDA has a list of guidelines and ingredients commonly referred to as the GRAS list (Generally Recognized as Safe). Ingredients on this list are considered to be pre-approved. All the ingredients in To Your Health are on this list or fall into their pre-approved guidelines.

The Homeopathic Pharmacopoeia Convention of the United States is responsible for establishing good manufacturing procedures and industry standards in collaboration with the FDA. The FDA does not use the same standards for approval of homeopathic medicines as it does for conventional drugs due to the overwhelming safety record of the homeopathic approach and extreme dilutions.

Americaloe, a subsidiary of SEASILVER USA, produces Seasilver. Americaloe only produces Seasilver and only produces it for Seasilver USA. Americaloe is licensed and approved by the FDA to produce dietary supplements.

Our products are nutritional supplements, not drugs. PHENOLMENAL! Balance? and BalanceDrops? are governed by the Dietary Supplement Health & Education Act, a federal law which governs the supplement market. TBC strictly adheres to all applicable law in this regard, and rigorously tests its products for quality and safety prior to sale.

Yes. Our certification is updated each year. Visit our Visit out quality assurance section for more information about our FDA certification.

From time to time the FDA or other government agencies will detain and inspect parcels from various sources being imported into the US or other countries. This is part of their routine. If a package is held they should immediately send a letter by Regular Post to the intended recipient with a contact number. This may take up to 10 days to arrive. The FDA should return the medication package to the dispensing pharmacy.

Laser beams concentrate their energy into a tiny space. If their energy content isn't limited, lasers can damage vision or even cause blindness. The FDA classifies lasers based upon how much power they emit. Class IIIa lasers are those that produce no more than 5 milliwatts of power; the limit deemed safe for unregulated use in public places. All Jasper lasers are Class IIIa.

Yes. The FDA announced on November 15, 2002, that it had received about 20 reports of serious reactions, including skin diseases Stevens Johnson Syndrome (SJS), toxic epidermal necrolysis (TEN), exfoliative dermatitis, and erythemamutliforme (EM)] and hypersensitivity reactions (anaphylactic reactions and angioedema). Pharmacia had issued a Dear Healthcare Professional letter two days earlier regarding these conditions.