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BURNR

BURNR

$59.99

ADVANCED THERMOGENIC FAT BURNER

  • Increase Metabolic Rate*
  • Activate Lipolysis*
  • Enhance Fat Burning*
  • Reduce Body Weight*
  • Control Appetite*
  • 60 Servings

 

About

Losing fat sounds so easy when it’s broken down. Eat less. Move more. Yeah, yeah. Can we get that in a pill form?

No. The truth of the matter is you cannot. Not yet, anyway; though science will get us there at some point. The next best thing? That’s BURNR. A one-stop shop for increased resting metabolism and enhanced body fat burning.

  • Caffeine – At the dose found in BURNR, caffeine provides a huge boost to metabolic rate while also enhancing fat oxidation.
  • 5-HTP – Helps reduce appetite, making dieting easier and reducing related stress.
  • TeaCrine™ – Boosts attention, energy, and mood – helpful even when not dieting!
  • CapsiAtra™ Dihydrocapsiate – Offers potent, broad-scale molecular weight loss by improving insulin sensitivity, reducing fat storage, and activating lipolysis.
  • Octopalean™ - Behaves similarly to synephrine and epinephrine to drive fat loss.

It’s going to take a full-scale assault to achieve meaningful changes in body fat and body weight. This means diet, exercise, and the help of a quality fat BURNR.

 

*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Supplement Facts

 Best fat burner

Ingredients

Niacin

Niacin is vitamin B3.

  • Promotes nervous system, skin, digestive, and eye health
  • Helps the liver metabolize foods and assists in the production of sex hormones
  • May increase blood circulation

 

Vitamin B6

A water-soluble vitamin also known as pyridoxine.

  • Helps manage cholesterol
  • Participates in nutrient metabolism by activating coenzymes.

 

Chromium

A trace mineral required for several bodily functions.

  • Helps shuttle blood glucose into cells to be used as energy
  • May help regulate fat and cholesterol.
  • Assists in controlling hunger

 

Caffeine Anhydrous + Infinergy™

Well-known stimulant for boosting energy and focus.

  • Increases total daily caloric expenditure by as much as 400 calories per day with a single dose
  • Infinergy helps extend caffeine’s effects and prevent crashing
  • Robustly enhances endurance performance
  • Activates fat oxidation

 

Grains of Paradise

This ingredient is a pioneer in addressing the new frontier of brown adipose tissue, a dynamic and thermogenic type of body fat.

  • Activates brown fat cells, which increase uncoupling proteins and calorie burn.
  • A recent study has found that grains of paradise significantly increase thermogenesis

 

Octopamine (as Octopalean™)

Chemically similar to synephrine and epinephrine, octopamine helps augment fatty acid balance.

  • Reduces creation of new fat cells
  • Increases body fat oxidation

 

GBB

Gamma-butyrobetaine ethyl ester chloride (GBB) is a precursor to carnitine.

  • Induces diaphoresis – aka intense sweating
  • As a precursor to carnitine, GBB is more efficiently absorbed leading to greater carnitine (fat transporter) levels

 

Rauwolscine

Also known as alpha-yohimbine, rauwolscine helps boost fat loss by antagonizing alpha adrenergic receptors.

  • The alpha adrenergic receptors are densest around common weight loss problem areas, like the thighs and waist.
  • Supplementing with or using topical yohimbine has been found to be effective for reducing fat in these areas.
  • Helps potentiate fat loss by other stimulants.

 

CapsiAtra

CapsiAtra contains dihydrocapsiate, a bioactive of peppers with effects on fat loss.

  • Behaves similarly to thyroid hormones for inducing weight loss
  • Reduces fat storage while promoting body fat release
  • Increases metabolic rate

 

Hordenine

Found alongside synephrine in bitter orange, hordenine is an adrenaline reuptake inhibitor.

  • As an adrenaline reuptake inhibitor, the adrenaline release from caffeine is prolonged and more effective.
  • As bitter orange, helps suppress body fat accumulation
  • As bitter orange, reduces waist and hip girths

 

Beta-Phenylethylamine

A natural neuromodulator.

  • Helps release dopamine and other neurotransmitters.
  • Improves mood and concentration
  • May speed up metablism

 

TeaCrine

Theacrine helps provide optimal release of neurotransmitters for sustained attention and mood.

  • Increases dopamine and adenosine.
  • May increase metabolism, energy production, focus, and mood.

 

GABA

GABA is a “downer” neurotransmitter that may also increase growth hormone.

  • Helps reduce anxiety
  • May improve exercise performance

 

Cytidine 5’-diphosphocholine

Also known as CDP choline. This form of choline is the best for nootropic benefits.

  • Converts to choline and uridine
  • Enhances memory and focus

 

Alpha Lipoic Acid

A fatty acid of mitochondrial importance.

  • Provides appetite suppression
  • Anti-oxidant helps protect

 

5-HTP

Serves as a precursor to serotonin.

  • Helps control hunger
  • May enhance the anabolic response to weight training
  • Experiments supplementing participants with 5-HTP has helped reduce their calorie intake by 38%, which lead to significant reductions in body weight.

 

Cassia

Cassia is a type of cinnamon.

  • Helps manage blood glucose and improves insulin function.
  • May reduce gastrointestinal distress
  • May help manage blood lipids.
FAQ

Q: What is the best way to use BURNR?

A: As a dietary supplement, take 1 serving (1 capsule) in the morning or before cardiovascular activity. Do not consume more than 1 capsule at a time or 2 capsules in a 24 hour period.

 

Q: Can I stack other products with BURNR?

A: Yes. BURNR can be stacked with RECOMP and CORTX for total body composition enhancement.

References

Vitamin B3 (Niacin):
1.    Elam, M. B., Hunninghake, D. B., Davis, K. B., Garg, R., Johnson, C., Egan, D., ... & ADMIT Investigators. (2000). Effect of niacin on lipid and lipoprotein levels and glycemic control in patients with diabetes and peripheral arterial disease: the ADMIT study: a randomized trial. Jama,284(10), 1263-1270.

2.    Goldberg, A., Alagona, P., Capuzzi, D. M., Guyton, J., Morgan, J. M., Rodgers, J., ... & Samuel, P. (2000). Multiple-dose efficacy and safety of an extended-release form of niacin in the management of hyperlipidemia. The American journal of cardiology, 85(9), 1100-1105.

3.    Guyton, J. R. (2007). Niacin in cardiovascular prevention: mechanisms, efficacy, and safety. Current opinion in lipidology, 18(4), 415-420.

Vitamin B6 (Pyridoxine):
1.    Czaja, J., Lebiedzinska, A., Marszall, M., & Szefer, P. (2011). Evaluation for magnesium and vitamin B6 supplementation among Polish elite athletes.Roczniki Państwowego Zakładu Higieny, 62(4).

2.    Manore, M. M. (2000). Effect of physical activity on thiamine, riboflavin, and vitamin B-6 requirements. The American journal of clinical nutrition, 72(2), 598s-606s.

3.    https://vitaminb6benefits.com/vitamin-b6-benefits

Chromium (Chromium Polynicotinate):
1.    Parsons A, et al. A proof of concept randomised placebo controlled factorial trial to examine the efficacy of St John's wort for smoking cessation and chromium to prevent weight gain on smoking cessation. Drug Alcohol Depend. (2009)

2.    Abdollahi M, et al. Effect of chromium on glucose and lipid profiles in patients with type 2 diabetes; a meta-analysis review of randomized trials. J Pharm Pharm Sci. (2013)

3.    Martin J, et al. Chromium picolinate supplementation attenuates body weight gain and increases insulin sensitivity in subjects with type 2 diabetes. Diabetes Care. (2006)

4.    J Nutr Biochem. 2012 Apr;23(4):313-9. doi: 10.1016/j.jnutbio.2011.11.001. Molecular mechanisms of chromium in alleviating insulin resistance. Hua Y, Clark S, Ren J, Sreejayan N. College of Health Sciences, School of Pharmacy, Center for Cardiovascular Research and Alternative Medicine, University of Wyoming, Laramie, WY 82071, USA.

5.    R. I. Press, J. Geller, and G. W. Evans The effect of chromium picolinate on serum cholesterol and apolipoprotein fractions in human subjects.

6.    Harry G. Preuss1,*, Nadeem Talpur1, Vijaya Manohar1, Nagaveni Venkataramiah1 and Richard A. Anderson Chromium and hypertension

7.    Stephen D. Anton, Christopher D. Morrison, William T. Cefalu, Corby K. Martin, Sandra Coulon, Paula Geiselman, Hongmei Han, Christy L. White, and Donald A. Williamson. Effects of Chromium Picolinate on Food Intake and Satiety 

Caffeine Matrix (Caffeine Anhydrous, DiCaffeine Malate):
1.    Goldstein, E. R., Ziegenfuss, T., Kalman, D., Kreider, R., Campbell, B., Wilborn, C., ... & Wildman, R. (2010). International society of sports nutrition position stand: caffeine and performance. J Int Soc Sports Nutr, 7(1), 5.

2.    Spriet, L. L. (1995). Caffeine and performance. International journal of sport nutrition, 5, S84-S84.

3.    Beck, T. W., Housh, T. J., Schmidt, R. J., Johnson, G. O., Housh, D. J., Coburn, J. W., & Malek, M. H. (2006). The acute effects of a caffeine-containing supplement on strength, muscular endurance, and anaerobic capabilities. The Journal of Strength & Conditioning Research, 20(3), 506-510.

4.    McLellan, T. M., Kamimori, G. H., Voss, D. M., Tate, C., & Smith, S. J. (2007). Caffeine effects on physical and cognitive performance during sustained operations. Aviation, space, and environmental medicine, 78(9), 871-877.

5.    Lieberman, H. R., Tharion, W. J., Shukitt-Hale, B., Speckman, K. L., & Tulley, R. (2002). Effects of caffeine, sleep loss, and stress on cognitive performance and mood during US Navy SEAL training. Psychopharmacology, 164(3), 250-261.

6.    Costill, D. L., Dalsky, G. P., & Fink, W. J. (1977). Effects of caffeine ingestion on metabolism and exercise performance. Medicine and science in sports, 10(3), 155-158.

7.    Kovacs, E. M., Stegen, J. H., & Brouns, F. (1998). Effect of caffeinated drinks on substrate metabolism, caffeine excretion, and Performance. Journal of Applied physiology, 85(2), 709-715.

Octopamine

1.    Roeder, T. (2005). Tyramine and octopamine: ruling behavior and metabolism.  Rev. Entomol., 50, 447-477.

2.    David, J. C., & Coulon, J. F. (1985). Octopamine in invertebrates and vertebrates. A review. Progress in neurobiology, 24(2), 141-185.

3.    Visentin, V., Morin, N., Fontana, E., Prévot, D., Boucher, J., Castan, I., ... & Carpéné, C. (2001). Dual action of octopamine on glucose transport into adipocytes: inhibition via β3-adrenoceptor activation and stimulation via oxidation by amine oxidases. Journal of Pharmacology and Experimental Therapeutics, 299(1), 96-104.

4.    Pizzinat, N., Marti, L., Remaury, A., Leger, F., Langin, D., Lafontan, M., ... & Parini, A. (1999). High expression of monoamine oxidases in human white adipose tissue: evidence for their involvement in noradrenaline clearance. Biochemical pharmacology, 58(11), 1735-1742.

5.    Marti, L., Morin, N., Enrique-Tarancon, G., Prevot, D., Lafontan, M., Testar, X., ... & Carpéné, C. (1998). Tyramine and vanadate synergistically stimulate glucose transport in rat adipocytes by amine oxidase-dependent generation of hydrogen peroxide. Journal of Pharmacology and Experimental Therapeutics, 285(1), 342-349.

6.    Fontana, E., Morin, N., Prévot, D., & Carpéné, C. (2000). Effects of octopamine on lipolysis, glucose transport and amine oxidation in mammalian fat cells. Comparative Biochemistry and Physiology Part C: Pharmacology, Toxicology and Endocrinology, 125(1), 33-44.


Aframomum melegueta:
1.    Sugita, J., Yoneshiro, T., Hatano, T., Aita, S., Ikemoto, T., Uchiwa, H., ... & Saito, M. (2013). Grains of paradise (Aframomum melegueta) extract activates brown adipose tissue and increases whole-body energy expenditure in men. British Journal of Nutrition, 110(04), 733-738.

2.    Iwami, M., Mahmoud, F. A., Shiina, T., Hirayama, H., Shima, T., Sugita, J., & Shimizu, Y. (2011). Extract of grains of paradise and its active principle 6-paradol trigger thermogenesis of brown adipose tissue in rats. Autonomic Neuroscience, 161(1), 63-67.

Green Coffee Bean Extract:
1.    Taylor, L. W., Wilborn, C. D., Harvey, T., Wismann, J., & Willoughby, D. S. (2007). Acute effects of ingesting Java Fit™ energy extreme functional coffee on resting energy expenditure and hemodynamic responses in male and female coffee drinkers. Journal of the International Society of Sports Nutrition, 4(1), 1-9.

2.    Shimoda, H., Seki, E., & Aitani, M. (2006). Inhibitory effect of green coffee bean extract on fat accumulation and body weight gain in mice. BMC complementary and alternative medicine, 6(1), 1.

3.    Burke, A., Catalano, P., Lal, S. K., Maniam, P., & Tojino, C. Green Coffee Bean Extract.

4.    Watanabe, T., Arai, Y., Mitsui, Y., Kusaura, T., Okawa, W., Kajihara, Y., & Saito, I. (2006). The blood pressure-lowering effect and safety of chlorogenic acid from green coffee bean extract in essential hypertension. Clinical and experimental hypertension, 28(5), 439-449.

5.    Onakpoya, I., Terry, R., & Ernst, E. (2010). The use of green coffee extract as a weight loss supplement: a systematic review and meta-analysis of randomized clinical trials. Gastroenterology research and practice, 2011.

Rauwolscine:
1.    Perry, B. D., & U'Prichard, D. C. (1981). [3 H] Rauwolscine (α-yohimbine): A specific antagonist radioligand for brain α 2-adrenergic receptors. European journal of pharmacology, 76(4), 461-464.

2.    Rockhold, R. W., & Gross, F. (1981). Yohimbine diastereoisomers: Cardiovascular effects after central and peripheral application in the rat.Naunyn-Schmiedeberg's archives of pharmacology, 315(3), 227-231.

3.    Arthur, J. M., Casańas, S. J., & Raymond, J. R. (1993). Partial agonist properties of rauwolscine and yohimbine for the inhibition of adenylyl cyclase by recombinant human 5-HT 1A receptors. Biochemical pharmacology,45(11), 2337-2341.

4.    Wainscott, D. B., Sasso, D. A., Kursar, J. D., Baez, M., Lucaites, V. L., & Nelson, D. L. (1997). [3H] Rauwolscine: an antagonist radioligand for the cloned human 5-hydroxytryptamine2B (5-HT2B) receptor. Naunyn-Schmiedeberg's archives of pharmacology, 357(1), 17-24.

CapsiAtra™ (Dihydrocapsiate):

1.    Galgani, J. E., & Ravussin, E. (2010). Effect of dihydrocapsiate on resting metabolic rate in humans. The American journal of clinical nutrition, 92(5), 1089-1093.

2.    Lee, T. A., Li, Z., Zerlin, A., & Heber, D. (2010). Effects of dihydrocapsiate on adaptive and diet-induced thermogenesis with a high protein very low calorie diet: a randomized control trial. Nutrition & metabolism, 7(1), 1.

3.    Galgani, J. E., Ryan, D. H., & Ravussin, E. (2010). Effect of capsinoids on energy metabolism in human subjects. British journal of nutrition, 103(01), 38-42.

4.    Inoue, N., Matsunaga, Y., Satoh, H., & Takahashi, M. (2007). Enhanced energy expenditure and fat oxidation in humans with high BMI scores by the ingestion of novel and non-pungent capsaicin analogues (capsinoids). Bioscience, biotechnology, and biochemistry, 71(2), 380-389.

Beta-Phenylethylamine:
1.    Sabelli HC, Borison RL, Diamond BI, Havdala HS, Narasimhachari N. Phenylethylamine and brain function. Biochem Pharmacol. 1978

2.    Calvert R, Vohra S, Ferguson M, Wiesenfeld P. A beating heart cell model to predict cardiotoxicity: effects of the dietary supplement ingredients higenamine, phenylethylamine, ephedrine and caffeine. Food Chem Toxicol. 2015

3.    Greenshaw AJ. Functional interactions of 2-phenylethylamine and of tryptamine with brain catecholamines: implications for psychotherapeutic drug action. Prog Neuropsychopharmacol Biol Psychiatry. 1989

4.    Nieforth KA. Psychotomimetic phenethylamines. J Pharm Sci. 1971

5.    Heuson E, Storgaard M, Huynh TH, Charmantray F, Gefflaut T, Bunch L. Profiling substrate specificity of two series of phenethylamine analogs at monoamine oxidase A and B. Org Biomol Chem. 2014

6.    Boulton AA, Juorio AV, Paterson IA. Phenylethylamine in the CNS: effects of monoamine oxidase inhibiting drugs, deuterium substitution and lesions and its role in the neuromodulation of catecholaminergic neurotransmission. J Neural Transm Suppl. 1990

Theacrine:

1.    Habowski, S. M., Sandrock, J. E., Kedia, A. W., & Ziegenfuss, T. N. (2014). The effects of TeacrineTM, a nature-identical purine alkaloid, on subjective measures of cognitive function, psychometric and hemodynamic indices in healthy humans: a randomized, double-blinded crossover pilot trial. Journal of the International Society of Sports Nutrition, 11(1), 1-2.

2.    Taylor, L., Mumford, P., Roberts, M., Hayward, S., Mullins, J., Urbina, S., & Wilborn, C. (2016). Safety of TeaCrine®, a non-habituating, naturally-occurring purine alkaloid over eight weeks of continuous use. Journal of the International Society of Sports Nutrition, 13(1), 1-14.

3.    Kuhman, D. J., Joyner, K. J., & Bloomer, R. J. (2015). Cognitive Performance and Mood Following Ingestion of a Theacrine-Containing Dietary Supplement, Caffeine, or Placebo by Young Men and Women.Nutrients, 7(11), 9618-9632.

GABA:

1.    Cavagnini, F., Invitti, C., Pinto, M., Maraschini, C., Di Landro, A., Dubini, A., & Marelli, A. (1980). Effect of acute and repeated administration of gamma aminobutyric acid (GABA) on growth hormone and prolactin secretion in man. Acta endocrinologica, 93(2), 149-154.

2.    Cavagnini, F., Invitti, C., Di Landro, A., Tenconi, L., Maraschini, C., & Girotti, G. (1977). Effects of a gamma aminobutyric acid (GABA) derivative, baclofen, on growth hormone and prolactin secretion in man. The Journal of Clinical Endocrinology & Metabolism, 45(3), 579-584.

3.    Cavagnini, F., Pinto, M., Dubini, A., Invitti, C., Cappelletti, G., & Polli, E. E. (1982). Effects of gamma aminobutyric acid (GABA) and muscimol on endocrine pancreatic function in man. Metabolism, 31(1), 73-77.

4.    Inoue, K., Shirai, T., Ochiai, H., Kasao, M., Hayakawa, K., Kimura, M., & Sansawa, H. (2003). Blood-pressure-lowering effect of a novel fermented milk containing γ-aminobutyric acid (GABA) in mild hypertensives. European Journal of Clinical Nutrition, 57(3), 490-495.

5.    Powers, M. E., Yarrow, J. F., McCoy, S. C., & Borst, S. E. (2008). Growth hormone isoform responses to GABA ingestion at rest and after exercise. Medicine and science in sports and exercise, 40(1), 104.

Cytidine 5’-diphosphocholine:

1.    McGlade, E., Locatelli, A., Hardy, J., Kamiya, T., Morita, M., Morishita, K., ... & Yurgelun-Todd, D. (2012). Improved attentional performance following citicoline administration in healthy adult women. Food and Nutrition Sciences, 3(6), 769.

2.    McGlade, E., Agoston, A. M., DiMuzio, J., Kizaki, M., Nakazaki, E., Kamiya, T., & Yurgelun-Todd, D. (2015). The Effect of Citicoline Supplementation on Motor Speed and Attention in Adolescent Males. Journal of attention disorders, 1087054715593633.

3.    Grieb, P. (2015). Citicoline: A Food That May Improve Memory. Medical Science Monitor Basic Research, 2, 67-72.

4.    Spiers, P. A., Myers, D., Hochanadel, G. S., Lieberman, H. R., & Wurtman, R. J. (1996). Citicoline improves verbal memory in aging. Archives of neurology, 53(5), 441-448.

Alpha Lipoic Acid:

1.    McNeilly, A. M., Davison, G. W., Murphy, M. H., Nadeem, N., Trinick, T., Duly, E., ... & McEneny, J. (2011). Effect of α-lipoic acid and exercise training on cardiovascular disease risk in obesity with impaired glucose tolerance. Lipids in health and disease, 10(1), 1.

2.    Zembron-Lacny, A., Slowinska-Lisowska, M., Szygula, Z., Witkowski, K., Stefaniak, T., & Dziubek, W. (2009). Assessment of the antioxidant effectiveness of alpha-lipoic acid in healthy men exposed to muscle-damaging exercise. J Physiol Pharmacol, 60(2), 139-43.

3.    Sola, S., Mir, M. Q., Cheema, F. A., Khan-Merchant, N., Menon, R. G., Parthasarathy, S., & Khan, B. V. (2005). Irbesartan and lipoic acid improve endothelial function and reduce markers of inflammation in the metabolic syndrome results of the irbesartan and lipoic acid in endothelial dysfunction (island) study. Circulation, 111(3), 343-348.

4.    Ranieri, M., Sciuscio, M., Cortese, A. M., Santamato, A., Di Teo, L., Ianieri, G., ... & Megna, M. (2009). The Use and Alpha-Lipoic Acid (ALA), Gamma Linolenic Acid (GLA) and Rehabilitation in the Treatment of Back Pain: Effect on Health-Related Quality of Life. International journal of immunopathology and pharmacology, 22(3 suppl), 45-50.

5-HTP:

1.    Rondanelli M, et al. Relationship between the absorption of 5-hydroxytryptophan from an integrated diet, by means of Griffonia simplicifolia extract, and the effect on satiety in overweight females after oral spray administration. Eat Weight Disord. (2012)

2.     Birdsall TC. 5-Hydroxytryptophan: a clinically-effective serotonin precursor. Altern Med Rev. (1998)

3.     Ceci F, et al. The effects of oral 5-hydroxytryptophan administration on feeding behavior in obese adult female subjects. J Neural Transm. (1989)

4.     Effects of oral 5-hydroxy-tryptophan on energy intake and macronutrient selection in non-insulin dependent diabetic patients. Int J Obes Relat Metab Disord. (1998)

5.    Wurtman RJ, Wurtman JJ. Brain serotonin, carbohydrate-craving, obesity and depression. Obes Res. (1995)

6.     Schruers K, et al. Acute L-5-hydroxytryptophan administration inhibits carbon dioxide-induced panic in panic disorder patients. Psychiatry Res. (2002)

7.     Aliño JJ, Gutierrez JL, Iglesias ML. 5-Hydroxytryptophan (5-HTP) and a MAOI (nialamide) in the treatment of depressions. A double-blind controlled study. Int Pharmacopsychiatry. (1976)

8.     Kline N, Sacks W. Treatment of depression with an mao inhibitor followed by 5-HTP--an unfinished research project. Acta Psychiatr Scand Suppl. (1980)

Cassia:

1.    Solomon et al. Effects of short-term cinnamon ingestion on in vivo glucose tolerance. Diabetes Obes Metab. 2007 Nov;9(6):895-901.

2.    Solomon et al. Changes in glucose tolerance and insulin sensitivity following 2 weeks of daily cinnamon ingestion in healthy humans. Eur J Appl Physiol. 2009 Apr;105(6):969-76. doi: 10.1007/s00421-009-0986-9. Epub 2009 Jan 22.

3.    Vafa et al. Effects of cinnamon consumption on glycemic status, lipid profile and body composition in type 2 diabetic patients. Int J Prev Med. 2012 Aug;3(8):531-6.

4.    Lee et al. Immunomodulatory effect of water extract of cinnamon on anti-CD3-induced cytokine responses and p38, JNK, ERK1/2, and STAT4 activation. Immunopharmacol Immunotoxicol. 2011 Dec;33(4):714-22. doi: 10.3109/08923973.2011.564185. Epub 2011 Mar 29. PMID:22053946

5.    Kumar et al. GC-MS analysis and screening of antidiabetic, antioxidant and hypolipidemic potential ofCinnamomum tamala oil in streptozotocin induced diabetes mellitus in rats. Cardiovasc Diabetol. 2012 Aug 10;11:95. doi: 10.1186/1475-2840-11-95. PMID:22882757

 

WARNING

California’s Proposition 65 entitles California consumers to special warnings.

WARNING: Cancer and Reproductive Harm - www.P65warnings.ca.gov/