Proper blood cleansing can have a profound impact on your health. Baseline Nutritionals'® Blood Support™ supplement provides Blood Purifier and Blood Cleansing Benefits.
- Supports the body's ability to support normal cellular growth.
- Powerful blood purifier and lymph cleanser promotes optimum health.
- Made with all organic, wild crafted, and/or ethically imported herbs.
- Watch Video - How To Cleanse Your Blood
Blood Support™ is best used as part of our Kidney/Liver/Gallbladder/Blood Detox Package.
Blood Support incorporates the most powerful blood cleansing herbs known to man. Burdock root, goldenseal root and bloodroot work to help remove toxic residues that naturally form in the blood, thus promoting optimum liver health, while at the same time supporting your blood’s natural protective properties. *
Ingredient Supporting Studies:
1. "Cancer Facts and Figures 2014." American Cancer Society. (Accessed 5 June 2014.) http://www.cancer.org/acs/groups/content/@research/documents/webcontent/acspc-042151.pdf
2. Sheikh, N. M.; Philen, R. M.; Love, L. A. "Chaparral-associated hepatotoxicity." Arch Intern Med, 157(8), 913-919. http://www.accessdata.fda.gov/scripts/Plantox/Detail.CFM?ID=28
3. Dafna W. Gordon, Gayle Rosenthal, John Hart, et al. "Chaparral Ingestion, the Broadening Spectrum of Liver Injury Caused by Herbal Medications." JAMA. 1995;273(6):489-490.
4. Watts, C. “Final Report to the American Herbal Products Association.” Special Counsel, Ford and Ferraro, LLP, Austin, TX. 6 Sept 1994. Unfortunately, there do not appear to be any internet accessible copies available at this time.
5. SILENA HERON, N.D., and ERIC YARNELL, N.D. "The Safety of Low-Dose Larrea tridentata (DC) Coville (Creosote Bush or Chaparral): A Retrospective Clinical Study. THE JOURNAL OF ALTERNATIVE AND COMPLEMENTARY MEDICINE. Volume 7, Number 2, 2001, pp. 175–185 http://larrearx.com/images/JournalofAlternativeMedSafetyofLarrea.pdf
6. Lü JM, Nurko J, Weakley SM, Jiang J, et al. "Molecular mechanisms and clinical applications of nordihydroguaiaretic acid (NDGA) and its derivatives: an update." Med Sci Monit. 2010 May;16(5):RA93-100. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2927326/
7. Hwu JR1, Hsu CI, Hsu MH, Liang YC, Huang RC, Lee YC. "Glycosylated nordihydroguaiaretic acids as anti-cancer agents." Bioorg Med Chem Lett. 2011 Jan 1;21(1):380-2. http://www.ncbi.nlm.nih.gov/pubmed/21123067
8. Hsu MH1, Wu SC, Pao KC, Unlu I, et al. "Hepatocellular carcinoma targeting agents: conjugates of nitroimidazoles with trimethyl nordihydroguaiaretic Acid." ChemMedChem. 2014 May;9(5):1030-7. http://www.ncbi.nlm.nih.gov/pubmed/24648164
9. Zhang Y1, Xu S, Lin J, Yao G, Han Z, Liang B, et al. "mTORC1 is a target of nordihydroguaiaretic acid to prevent breast tumor growth in vitro and in vivo." Breast Cancer Res Treat. 2012 Nov;136(2):379-88. http://www.ncbi.nlm.nih.gov/pubmed/23053656
10. Ryan CJ1, Zavodovskaya M, Youngren JF, Campbell M, Diamond M, Jones J, Shiry L, et al. "Inhibitory effects of nordihydroguaiaretic acid (NDGA) on the IGF-1 receptor and androgen dependent growth of LAPC-4 prostate cancer cells." Prostate. 2008 Aug 1;68(11):1232-40. http://www.ncbi.nlm.nih.gov/pubmed/18491370
11. Chen H1, Teng L, Li JN, Park R, Mold DE, et al. "Antiviral activities of methylated nordihydroguaiaretic acids. 2. Targeting herpes simplex virus replication by the mutation insensitive transcription inhibitor tetra-O-methyl-NDGA."J Med Chem. 1998 Jul 30;41(16):3001-7. http://www.ncbi.nlm.nih.gov/pubmed/9685239
12. Zhao J1, Zhao Y, Chen W, Li YM, Bian XW. "The differentiation-inducing effect of Nordy on HPV-16 subgenes-immortalized human endocervical cells H8." Anticancer Drugs. 2008 Aug;19(7):713-9. http://www.ncbi.nlm.nih.gov/pubmed/18594213
13. Gao P1, Zhai F, Guan L, Zheng J. "Nordihydroguaiaretic acid inhibits growth of cervical cancer SiHa cells by up-regulating p21."Oncol Lett. 2011 Jan;2(1):123-128. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3412500/
14. Peterson G1, Barnes S. "Genistein and biochanin A inhibit the growth of human prostate cancer cells but not epidermal growth factor receptor tyrosine autophosphorylation." Prostate. 1993;22(4):335-45. http://www.ncbi.nlm.nih.gov/pubmed/8497428
15. Lai K. Leung, Ho Yee Chan, Huan Wang. "The red clover (Trifolium pratense) isoflavone biochanin A modulates the biotransformation pathways of 7,12-dimethylbenz[a]anthracene." British Journal of Nutrition / Volume 90 / Issue 01 / July 2003, pp 87-92. http://journals.cambridge.org/action/displayFulltext?type=6&fid=1044284&jid=BJN&volumeId=90&issueId=01&aid=1043644&fulltextType=RA&fileId=S0007114503002472
16. Wang Y, Man Gho W, Chan FL, Chen S, Leung LK. "The red clover (Trifolium pratense) isoflavone biochanin A inhibits aromatase activity and expression." Br J Nutr 2008;99(2):303-310. http://www.ncbi.nlm.nih.gov/pubmed/17761019
17. Mannella P, Tosi V, Russo E, et al. "Effects of red clover extracts on breast cancer cell migration and invasion." Gynecol endocrinol. 2012; 28(1):29-33. http://www.ncbi.nlm.nih.gov/pubmed/21615235
18. Stephens FO. "Phytoestrogens and prostate cancer: possible preventive role." MJA. 1997;167:138-140. http://www.ncbi.nlm.nih.gov/pubmed/9269268
19. Jarred RA, Keikha M, Dowling C, et al. "Induction of apoptosis in low to moderate-grade human prostate carcinoma by red clover-derived dietary isoflavones." Cancer Epidemiol Biomarkers Prev. 2002;11:1689-1696. http://cebp.aacrjournals.org/content/11/12/1689.full
20. Stephens F. O. Phytoestrogens and prostate cancer: possible preventive role. Med. J. Aust., 167: 138- 140, 1997. http://www.ncbi.nlm.nih.gov/pubmed/9269268
21. Zhao F, Wang L, Liu K. "In vitro anti-inflammatory effects of arctigenin, a lignan from Arctium lappa L., through inhibition on iNOS pathway." J Ethnopharmacol. 2009 Apr 21;122(3):457-62. http://www.ncbi.nlm.nih.gov/pubmed/19429312
22. Chan YS, Cheng LN, Wu JH, et al. "A review of the pharmacological effects of Arctium lappa (burdock)." Inflammopharmacology. 2011 Oct;19(5):245-54. http://www.ncbi.nlm.nih.gov/pubmed/20981575
23. Lin SC, et al. "Hepatoprotective effects of Arctium lappa Linne on liver injuries induced by chronic ethanol consumption and potentiated by carbon tetrachloride." J Biomed Sci 2002 Sep-Oct;9(5):401-9. http://www.ncbi.nlm.nih.gov/pubmed/12218354
24. Lu LC, Zhou W, Li ZH, et al. "Effects of arctiin on streptozotocin-induced diabetic retinopathy in Sprague-Dawley rats." Planta Med. 2012 Aug;78(12):1317-23. http://www.ncbi.nlm.nih.gov/pubmed/22753037
25. Hirose M, Yamaguchi T, Lin C, et al. "Effects of arctiin on PhIP-induced mammary, colon and pancreatic carcinogenesis in female Sprague-Dawley rats and MeIQx-induced hepatocarcinogenesis in male F344 rats." Cancer Lett. 2000 Jul 3;155(1):79-88. http://www.sciencedirect.com/science/article/pii/S0304383500004110
26. Huang K1, Li LA, Meng YG, You YQ, Fu XY, Song L. "Arctigenin Promotes Apoptosis in Ovarian Cancer Cells via the iNOS/NO/STAT3/Survivin Signalling." Basic Clin Pharmacol Toxicol. 2014 May 19. http://www.ncbi.nlm.nih.gov/pubmed/24842412cancer
27. Susanti S1, Iwasaki H, Inafuku M, Taira N, Oku H. "Mechanism of arctigenin-mediated specific cytotoxicity against human lung adenocarcinoma cell lines." Phytomedicine. 2013 Dec 15;21(1):39-46. http://www.ncbi.nlm.nih.gov/pubmed/24021157
28. Hsieh CJ, Kuo PL, Hsu YC, Huang YF, Tsai EM, Hsu YL. "Arctigenin, a dietary phytoestrogen, induces apoptosis of estrogen receptor-negative breast cancer cells through the ROS/p38 MAPK pathway and epigenetic regulation." Free Radic Biol Med. 2014 Feb;67:159-70. http://www.ncbi.nlm.nih.gov/pubmed/24140706
29. Ek O, Waurzyniak B, Myers DE, Uckun FM. "Antitumor activity of TP3(anti-p80)-pokeweed antiviral protein immunotoxin in hamster cheek pouch and severe combined immunodeficient mouse xenograft models of human osteosarcoma." Clin Cancer Res. 1998 Jul;4(7):1641-7. http://clincancerres.aacrjournals.org/content/4/7/1641.full.pdf
30. Anderson PM, Meyers DE, Hasz DE, Covalcuic K, et al. "In vitro and in vivo cytotoxicity of an anti-osteosarcoma immunotoxin containing pokeweed antiviral protein." Cancer Res. 55: 1321-7, 1995. http://cancerres.aacrjournals.org/content/55/6/1321.full.pdf
31. Qi L, Nett TM, Allen MC, et al. "Binding and cytotoxicity of conjugated and recombinant fusion proteins targeted to the gonadotropin-releasing hormone receptor." Cancer Res. 2004;64:2090-2095. http://cancerres.aacrjournals.org/content/64/6/2090.full
32. Wimer BM, Mann PL. "Mitogen immunotherapy for HIV infections exemplified by phytohemagglutinin and pokeweed mitogen." Cancer Biother Radiopharm. 2001;15:629--44. http://www.ncbi.nlm.nih.gov/pubmed/11190495
33. Fatih M Uckun, Larisa Rustamova, Alexei O Vassilev, et al. "CNS activity of Pokeweed Anti-viral Protein (PAP) in mice infected with Lymphocytic Choriomeningitis Virus (LCMV)." BMC Infect Dis. 2005; 5: 9. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC554105/
34. Wegiera M1, Smolarz HD, Bogucka-Kocka A. "Rumex L. species induce apoptosis in 1301, EOL-1 and H-9 cell lines." Acta Pol Pharm. 2012 May-Jun;69(3):487-99. http://www.ptfarm.pl/pub/File/Acta_Poloniae/2012/3/487.pdf
35. Rostock M, Huber R, Greiner T, Fritz P, Scheer R, Schueler J, Fiebig HH. "Anticancer activity of a lectin-rich mistletoe extract injected intratumorally into human pancreatic cancer xenografts." Anticancer Res. 2005 May-Jun;25(3B):1969-75. http://ar.iiarjournals.org/content/25/3B/1969.long
36. "Mistletoe Extracts (PDQ®) - Human Clinical Trials." National Cancer Institute. (Accessed 31 May 2014.) http://www.cancer.gov/cancertopics/pdq/cam/mistletoe/HealthProfessional/Page5#Section_35
37. Tröger W, Zdrale Z, Tišma N, Matijaševic M. "Additional Therapy with a Mistletoe Product during Adjuvant Chemotherapy of Breast Cancer Patients Improves Quality of Life: An Open Randomized Clinical Pilot Trial." Evid Based Complement Alternat Med. 2014;2014:430518. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3950471/
38. Adaramoye O, Amanlou M, Habibi-Rezaei M, Pasalar P, Ali MM. "Methanolic extract of African mistletoe (Viscum album) improves carbohydrate metabolism and hyperlipidemia in streptozotocin-induced diabetic rats." Asian Pac J Trop Med. 2012 Jun;5(6):427-33. http://www.ncbi.nlm.nih.gov/pubmed/22575973
39. Gray AM, Flatt PR. "Insulin-secreting activity of the traditional antidiabetic plant Viscum album (mistletoe)." J Endocrinol. 1999 Mar;160(3):409-14. http://joe.endocrinology-journals.org/content/160/3/409.full.pdf
40. Stephen S. Leonarda, Deborah Keilb, Tracey Mehlmanb, et al. "Essiac tea: Scavenging of reactive oxygen species and effects on DNA damage." Journal of Ethnopharmacology Volume 103, Issue 2, 16 January 2006, Pages 288--296. http://www.sciencedirect.com/science/article/pii/S0378874105006239
41. Soroush Sardari, Mohammad Ali Shokrgozar, Ghazaleh Ghavami. "Cheminformatics based selection and cytotoxic effects of herbal extracts." Toxicology in Vitro, Volume 23, Issue 7, October 2009, Pages 1412-1421. http://www.sciencedirect.com/science/article/pii/S0887233309001866
42. "What is the mechanism by which Cat's claw (Uncaria tomentosa) can increase the blood concentrations of the protease inhibitors, atazanavir (Reyataz), ritonavir (Norvir), saquinavir, (Invirase) used for the treatment of HIV?" Pharmacology Weekly. (Accessed 1 June 1014.) http://www.pharmacologyweekly.com/articles/cat-claw-herb-concentrations-protease-inhibitors-HIV
43. Kaiser S, Dietrich F, de Resende PE, Verza SG, Moraes RC, et al. "Cat's claw oxindole alkaloid isomerization induced by cell incubation and cytotoxic activity against T24 and RT4 human bladder cancer cell lines." Planta Med. 2013 Oct;79(15):1413-20. http://www.ncbi.nlm.nih.gov/pubmed/23975868
44. Dreifuss AA, Bastos-Pereira AL, Fabossi IA, Lívero FA, et al. "Uncaria tomentosa exerts extensive anti-neoplastic effects against the Walker-256 tumour by modulating oxidative stress and not by alkaloid activity." I. 2013;8(2):e54618. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3567083/
45. Rinner B, Li ZX, Haas H, Siegl V, Sturm S, Stuppner H, Pfragner R. "Antiproliferative and pro-apoptotic effects of Uncaria tomentosa in human medullary thyroid carcinoma cells." Anticancer Res. 2009 Nov;29(11):4519-28. http://ar.iiarjournals.org/content/29/11/4519.long
46. Pilarski R, Poczekaj-Kostrzewska M, Ciesiolka D, Szyfter K, Gulewicz K. "Antiproliferative activity of various Uncaria tomentosa preparations on HL-60 promyelocytic leukemia cells." Pharmacol Rep. 2007 Sep-Oct;59(5):565-72. http://www.if-pan.krakow.pl/pjp/pdf/2007/5_565.pdf
47. Sun M1, Liu C, Nadiminty N, Lou W, Zhu Y, et al. "Inhibition of Stat3 activation by sanguinarine suppresses prostate cancer cell growth and invasion." Prostate. 2012 Jan;72(1):82-9. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3938016/
48. Malikova J, Zdarilova A, Hlobilkova A. "Effects of sanguinarine and chelerythrine on the cell cycle and apoptosis." Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2006 Jul;150(1):5-12. http://mefanet.upol.cz/BP/2006/1/5.pdf
49. Haseeb Ahsan, Shannon Reagan-Shaw, Jorien Breur, Nihal Ahmad. "Sanguinarine induces apoptosis of human pancreatic carcinoma AsPC-1 and BxPC-3 cells via modulations in Bcl-2 family proteins." Cancer Letters Volume 249, Issue 2 , Pages 198-208, 8 May 2007. http://www.cancerletters.info/article/S0304-3835(06)00526-X/abstract
50. Shin Kim, Tae-Jin Lee, Jaechan Leem, Kyeong Sook Choi, Jong-Wook Park, and Taeg Kyu Kwon1. "Sanguinarine-induced apoptosis: Generation of ROS, down-regulation of Bcl-2, c-FLIP, and synergy with TRAIL." Journal of Cellular Biochemistry Volume 104, Issue 3, pages 895--907, 1 June 2008. http://onlinelibrary.wiley.com/doi/10.1002/jcb.21672/abstract
51. Kim JB, Yu JH, Ko E et al. "The alkaloid Berberine inhibits the growth of Anoikis-resistant MCF-7 and MDA-MB-231 breast cancer cell lines by inducing cell cycle arrest." Phytomedicine 17 (6): 436--40. PMID 19800775. http://www.ncbi.nlm.nih.gov/pubmed/19800775
52. Lin CC, Lin SY, Chung JG, Lin JP, Chen GW, Kao ST. "Down-regulation of cyclin B1 and up-regulation of Wee1 by berberine promotes entry of leukemia cells into the G2/M-phase of the cell cycle." Anticancer Research 26 (2A): 1097--104. http://ar.iiarjournals.org/content/26/2A/1097.long
53. Serafim TL, Oliveira PJ, Sardao VA, Perkins E, Parke D, Holy J. "Different concentrations of berberine result in distinct cellular localization patterns and cell cycle effects in a melanoma cell line." Cancer Chemotherapy and Pharmacology 61 (6): 1007--18. http://www.ncbi.nlm.nih.gov/pubmed/17661039
54. Pinto-Garcia L, Efferth T, Torres A, Hoheisel JD, Youns M. "Berberine Inhibits Cell Growth and Mediates Caspase-Independent Cell Death in Human Pancreatic Cancer Cells." Planta Medica 76 (11): 1155--61. http://www.ncbi.nlm.nih.gov/pubmed/20455200
55. Ho YT, Lu CC, Yang JS et al. (October 2009). "Berberine induced apoptosis via promoting the expression of caspase-8, -9 and -3, apoptosis-inducing factor and endonuclease G in SCC-4 human tongue squamous carcinoma cancer cells". Anticancer Research 29 (10): 4063--70. http://ar.iiarjournals.org/content/29/10/4063.long
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4 droppers (4mL) in 2 oz of juice as needed. Shake well before using.
For blood cleansing and liver detoxification, 4 droppers three times a day until bottle is used up.
|Serving Size:||4 droppers (4mL)|
|Servings per Container:||15|
|Amount per Serving:||1456mg Herb Weight Equivalence|
|Container Size:||2 fl oz (59mL)|
|Strength:||Herb Strength Ratio 1:2.75|
|Click ingredient for more information|
|Amount Per Serving||% Daily Value|
|Red Clover Herb +||N/A*||N/A*|
|Chaparral Leaf >||N/A*||N/A*|
|Burdock Root +||N/A*||N/A*|
|Fresh Poke Root >||N/A*||N/A*|
|Yellow Dock Root >||N/A*||N/A*|
|Goldenseal Root +||N/A*||N/A*|
|Oregon Grape Root >||N/A*||N/A*|
|Mistletoe Herb >||N/A*||N/A*|
|Cat's Claw Bark ~||N/A*||N/A*|
|Sheep Sorrel Herb +||N/A*||N/A*|
|Cayenne Fruit +||N/A*||N/A*|
|What Ethically Wild Crafted Means||-|
|Other ingredients: Grain alcohol (45-55% by volume), deionized water, d-Limonene|
This formula is a proprietary blend
+ Certified Organic
> Ethically Wild Crafted
~ Selectively Imported Herbs
All ingredients are either domestically sourced or selectively imported
* Daily Value Not Established
No materials used to produce this product are derived from or contain any Genetically Modified Organisms (GMOs)
All Vegan and Vegetarian Formula
Red Clover Herb
Red Clover has a long history of use as a medicinal herb. It's an excellent blood purifier that over time gradually cleanses the bloodstream and supports the circulatory system. But among classic herbalists, it is probably best known as one of the best herbs for supporting and maintaining cellular health.
Red Clover contains genistein that is the same biochemical considered to be the main active ingredient in soy. But red clover has a significant advantage over soy. It contains not just genistein, but significant levels (about ten times that found in soy) of all four main estrogenic isoflavones, including daidzein and genistein. In addition to isoflavones, red clover contains phytoestrogen compounds called coumestans -- in the form of biochanin and formononetin. Consuming red clover isoflavones results in higher blood levels of daidzein and genistein, moderate blood levels of biochanin, and low levels of formononetin - at about the same profile seen in the blood of vegetarians who consume a variety of legumes.
Note: Soy consumption, unlike red clove consumption, does not result in any increase in biochanin or formononetin in the blood.
Native Americans have used Chaparral leaf for centuries. Exactly how it works is open to debate, but some of its main actions are:
- Chaparral leaf is one of the most powerful anti-oxidants in nature. The primary biochemical responsible for this is NDGA (nordihydroguaiaretic acid) - so effective, it is often used as a food preservative.
- Chaparral leaf cleanses the lymph system.
- It is a powerful blood purifier.
- It cleanses the liver.
- It cleanses the urinary tract.
- Studies show that chaparral may also inhibit cell proliferation as well as DNA synthesis.
So how could such a beneficial herb be on everyone's blacklist?
According to the FDA, Chaparral: sold has been linked to serious liver damage. FDA has recorded two deaths and 10 cases of hepatitis or other liver abnormalities in users.
The reality, though, is that the evidence for chaparral liver toxicity is anecdotal. It is not the result of any double blind studies or of any clinical trials. For example, one of the cases the FDA likes to single out can be found in the Journal of the American Medical Association (273 (6):489). The details of the case concern a 60-year-old woman who developed jaundice and liver failure while taking one to two capsules of chaparral each day with a pinch of garlic in a tea made from nettle and chickweed. The authors of the JAMA article concluded it was the chaparral that caused the liver problems. What is fascinating is that the patient in question was also consuming atenolol, aspirin, was on a nitro patch, and occasional acetaminophen, as well as diltiazem hydrochloride - all drugs with profound hepatoxic potential. Amazingly, none of these other substances was even considered as a possible cause of the liver problems by the authors...or the FDA. What a surprise!
Nevertheless (and despite the fact that extensive studies on chaparral in the 1970s and 1980s were unable to find any hepatotoxic properties), in December of 1992, FDA Commissioner David Kessler announced, "The public should not purchase or consume chaparral."
After these allegations of liver toxicity by the FDA, manufacturers voluntarily restricted sales of chaparral for several years until the reports were investigated. Following a lengthy review, a panel of medical experts concluded "no clinical data was found... to indicate chaparral is inherently a hepatic toxin." In late 1994, this report was submitted to the FDA. The American Herbal Products Association (AHPA) now recommends the following Companies that offer products for sale for internal use that contain chaparral (Larrea tridentata) [should] provide labeling that contains the following informational language:
Rare reports of serious liver disease have been associated with ingestion of chaparral. Seek advice from a health care practitioner before use and, in so doing, inform them if you have had, or may have had, liver disease, frequently use alcoholic beverages, or are using any medications. Discontinue use and see a doctor if vomiting, fever, fatigue, abdominal pain, loss of appetite, or jaundice (e.g., dark urine, pale stools, yellow discoloration of the eyes) should occur.
So is this remarkable herb now sold freely in the marketplace and used to benefit ailing people all over the world? Hardly!
Search for "chaparral toxicity" on the web and you will see numerous articles still announcing the dangers of the herb (all citing the same cases from the early 90's.) Or try and buy chaparral in Canada or much of Europe. Right! The problem is that once an herb is labeled dangerous (even if disproved at a later date), the stigma remains - and is brought up over and over and over again...acquiring truth through repetition, if not fact.
Fortunately, despite the bad press, chaparral, or larrea, is at least available (for the time being) in the United States.
Burdock root is probably the most famous detoxifying agent in the herbal arsenal. Burdock root cleanses the blood by increasing the effectiveness of all of the body's elimination systems. Its diuretic effect helps the kidneys filter the blood. Burdock root helps push toxins out, and it also boosts the ability of the liver to remove toxins. The bottom line is that by addressing toxins through a variety of pathways, burdock root acts as a blood purifier with minimal side effects and with minimal stress to the body.
Fresh Poke Root
Poke root and Yellow dock root are both powerful blood purifiers and lymph cleansers, inciting and increasing the action of lymph glands throughout the entire body. Not surprisingly, both herbs are staples of many traditional herbal formulas.
Yellow Dock Root
Pokeroot and Yellow dock root are both powerful blood cleansers and lymph cleansers, inciting and increasing the action of lymph glands throughout the entire body. Not surprisingly, both herbs are staples of many traditional cellular support formulas.
Goldenseal root is a multi purpose type of herb that provides immune system support, and cleanses vital organs. Goldenseal root promotes the functioning capacity of the heart, the lymphatic and respiratory system, the liver, the spleen, the pancreas, and the colon.
Taken internally, Goldenseal root increases digestive secretions, astringes the mucous membranes that line the gut, and helps promote the body’s natural inflammatory response system. It also aids digestive health by promoting the production of saliva, bile, and other digestive enzymes. In addition it may control heavy menstrual bleeding by means of its astringent action.
Note: Goldenseal root should be taken on an "as needed" basis since it may upset the natural balance of fauna and flora in the intestine.
Oregon Grape Root
Oregon grape root is frequently used by herbalists for blood cleansing, and to stimulate the liver and gall bladder. In addition, Oregon grape root is used as a mild laxative.
Bloodroot has been researched and found to be a potent cellular support agent. In addition to laboratory tests, Bloodroot has been used to treat tens of thousands of people over the last century and a half. Note: Dr. Andrew Weil has stated that Bloodroot preparations can be used as an effective alternative to support healthy skin.
Mistletoe's use for cellular health is widespread in central Europe.
Cat's Claw Bark
The Ashaninka tribe of Peru uses for a variety of purposes, including to support cellular health. Other indigenous tribes use Cat's Claw as well. The Cashibo tribe of eastern Peru believes that Cat's Claw normalizes the body and have used it since ancient times to cleanse the system. Other documented indigenous uses in Peru include using Uncaria tomentosa for blood cleansing and for irregularity of the menstrual cycle.
Sheep Sorrel Herb
Rene Caisse, who popularized Essiac tea for cellular health, felt sheep sorrel was the most active fighter among all the herbs present in her formula. That viewpoint was seconded by Dr. Stock at Sloan-Kettering in New York. Dr. Shock studied sheep sorrel for over three year years. His conclusion was that sheep sorrel was a powerful blood purifier.
The potent, hot fruit of cayenne has been used as medicine for centuries. Cayenne is helpful for various conditions of the gastrointestinal tract, including temporary constipation (by stimulating peristalsis), upset stomach aches, cramping, and gas. Cayenne is also extremely beneficial for the circulatory system, helping to improve the elasticity of the walls of both the arterial and venous systems, maintaining normal blood platelet function, and working to help maintain normal blood pressure already within a normal range throughout the body. And finally, cayenne is used in many herbal formulas as a "driver" -- to "push" the other herbs in the formula into the blood stream more quickly
What Ethically Wild Crafted Means
Wild crafting is the practice of harvesting plants from their natural, or wild" habitat, for food or medicinal purposes. It means the plants are uncultivated, and harvesting takes place wherever they may be found. Ethical wild crafting means that the harvesting is done sustainably.
Grain alcohol (45-55% by volume)
Yes. The products that are Kosher are: Blood Support, Liver Flush Tea, Metal Magic, Warp Speed, Men’s Formula, Women’s Formula, Immunify, and Nutribody Protein.
Yes. First, you should finish the bottle you started for liver and blood cleansing, even if it runs a couple of days longer than the detox itself.