Research Forum

Forum Navigation
You need to log in to create posts and topics.

Nutrition labels do not have to label Poison/"Vitamin A" content any longer

The FDA has decided to make labeling for Vitamin A content "optional" for companies on the updated Nutrition Facts Labels on foods.  The National Institutes of Health (NIH) knows that Vitamin A is one of the most toxic of all the nutrients.  See below for the evidence.

It will be important to put a couple of things together here:

  • The FDA admits that Vitamin A deficiencies are now rare (see quote from their page below).  Why are we still fortifying foods then?
  • The NIH admits that Vitamin A is one of the most toxic vitamins, both in the short-term (acute) and long-term (chronic). See quote below.
  • How will people be able to avoid getting too much of the MOST TOXIC vitamin--Poison/"Vitamin A"--shown to cause distinct toxicity from solely food sources OR solely fortified sources, if labels don't have to show it any longer?
  • Scurvy (the disease associated with a lack of Vitamin C) is still present in 10-14% of adults in the US!  Vitamin C is distinctly protective against the oxidative damage caused by Poison/"Vitamin A".  Scurvy is still present, yet we're taking it off of labels?

If one was to put the pieces together:

  • Glyphosate/Roundup inhibits Poison/"Vitamin A" breakdown by the liver
    • Glyphosate is being found everywhere, in everyone to some extent
  • Poison/"Vitamin A" is coming into people from every direction and is encouraged ("eat a rainbow", organ meats, supplements, cod liver oil, skincare/cosmetics, etc.)
    • Nutrition Label Facts don't have to show Vitamin A content any longer, the most toxic of all the so-called "vitamins"
    • Nutrition Label Facts don't have to show Vitamin C content any longer, one of the most protective nutrients

If we put these together, one might start to think that there is a stealth campaign going on to poison the population.

Changes to the Nutrition Facts Label

The list of nutrients that are required or permitted to be declared is being updated. Vitamin D and potassium will be required on the label. Calcium and iron will continue to be required. Vitamins A and C will no longer be required but can be included on a voluntary basis.

 

8. Why are you no longer requiring vitamins A and C?

In the early 1990’s, American diets lacked Vitamins A and C, but now Vitamins A and C deficiencies in the general population are rare. Manufacturers are still able to list these vitamins voluntarily.

Vitamin A - Fact Sheet for Health Professionals

Health Risks from Excessive Vitamin A

Because vitamin A is fat soluble, the body stores excess amounts, primarily in the liver, and these levels can accumulate. Although excess preformed vitamin A can have significant toxicity (known as hypervitaminosis A), large amounts of beta-carotene and other provitamin A carotenoids are not associated with major adverse effects [38]. The manifestations of hypervitaminosis A depend on the size and rapidity of the excess intake. The symptoms of hypervitaminosis A following sudden, massive intakes of vitamin A, as with Arctic explorers who ate polar bear liver, are acute [39]. Chronic intakes of excess vitamin A lead to increased intracranial pressure (pseudotumor cerebri), dizziness, nausea, headaches, skin irritation, pain in joints and bones, coma, and even death [2,4,5]. Although hypervitaminosis A can be due to excessive dietary intakes, the condition is usually a result of consuming too much preformed vitamin A from supplements or therapeutic retinoids [3,5]. When people consume too much vitamin A, their tissue levels take a long time to fall after they discontinue their intake, and the resulting liver damage is not always reversible.

Observational studies have suggested an association between high intakes of preformed vitamin A (more than 1,500 mcg daily—only slightly higher than the RDA), reduced bone mineral density, and increased fracture risk [1,4,40]. However, the results of studies on this risk have been mixed, so the safe retinol intake level for this association is unknown.

Total intakes of preformed vitamin A that exceed the UL and some synthetic retinoids used as topical therapies (such as isotretinoin and etretinate) can cause congenital birth defects [2-4]. These birth defects can include malformations of the eye, skull, lungs, and heart [4]. Women who might be pregnant should not take high doses of vitamin A supplements [2].

Unlike preformed vitamin A, beta-carotene is not known to be teratogenic or lead to reproductive toxicity [1]. And even large supplemental doses (20–30 mg/day) of beta-carotene or diets with high levels of carotenoid-rich food for long periods are not associated with toxicity. The most significant effect of long-term, excess beta-carotene is carotenodermia, a harmless condition in which the skin becomes yellow-orange [1,25]. This condition can be reversed by discontinuing beta-carotene ingestion.

Supplementation with beta-carotene, with or without retinyl palmitate, for 5–8 years has been associated with an increased risk of lung cancer and cardiovascular disease in current and former male and female smokers and in male current and former smokers occupationally exposed to asbestos [27,41]. In the ATBC study, beta-carotene supplements (20 mg daily) were also associated with increased mortality, mainly due to lung cancer and ischemic heart disease [27]. The CARET study ended early, after the investigators found that daily beta-carotene (30 mg) and retinyl palmitate (25,000 IU) supplements increased the risk of lung cancer and cardiovascular disease mortality [41].

The FNB has established ULs for preformed vitamin A that apply to both food and supplement intakes [5]. The FNB based these ULs on the amounts associated with an increased risk of liver abnormalities in men and women, teratogenic effects, and a range of toxic effects in infants and children. The FNB also considered levels of preformed vitamin A associated with decreased bone mineral density, but did not use these data as the basis for its ULs because the evidence was conflicting. The FNB has not established ULs for beta-carotene and other provitamin A carotenoids [25]. The FNB advises against beta-carotene supplements for the general population, except as a provitamin A source to prevent vitamin A deficiency.

Dr. Garrett Smith, the "Nutrition Detective"
Licensed Naturopathic Physician (NMD) in Arizona
NutritionDetective.com, home of the Love Your Liver program
YouTube - FaceBook - Instagram - Twitter