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Evo Slim Ingredients

Evo Slim Ingredients: All Twenty Rows and Amounts

Evo Slim lists twenty active ingredients and prints an amount for every one.

Seven are vitamins and minerals, led by chromium at 67 mcg. Ten are botanicals, led by banaba at 25 mg. There is no proprietary blend.

See the full supplement facts panel.

Below, each row gets its printed amount, what it is there for, and the amount the published trials actually used. Where those two are far apart the page says so.

The shape of it

The Evo Slim panel, grouped so twenty rows can be held at once

The panel prints them in that order too: vitamins and minerals first, then the botanicals, then the rest.

Seven with a Daily Value

Vitamin C, vitamin E, biotin, magnesium, zinc, manganese, chromium. Ordinary nutritional amounts doing ordinary nutritional work.

Ten botanicals

Banaba, guggul, bitter melon, licorice, cinnamon, gymnema, yarrow, cayenne, juniper, white mulberry.

Three others

Vanadium as vanadyl sulfate, alpha lipoic acid, L-taurine.

Row by row

Every Evo Slim ingredient, with its evidence

Twenty cards, in the order the label prints them across its three groups.

Chromium

as chromium amino acid chelate67 mcg

The panel's highest declared Daily Value at 191%, and the row with the largest body of weight research behind it. A 2013 meta-analysis of randomised trials found a small average difference in body weight; the Cochrane review published the same year rated the evidence low quality and the effect uncertain. Both pooled trials dosing mostly 200 to 1,000 mcg a day, so 67 mcg sits below the studied range while still being a sensible nutritional amount. A separate exploratory trial looked at carbohydrate craving rather than weight, which is closer to what the seller's icon set is pointing at. The NIH fact sheet is the plainest summary of what chromium is for.

Banaba Extract

Lagerstroemia speciosa, leaf, 1% corosolic acid25 mg

The standardisation is the whole story of this row. Twenty-five milligrams at one per cent carries about a quarter of a milligram of corosolic acid, and the published review of banaba and corosolic acid describes human work using single doses roughly forty to two hundred times that. Banaba is named in the H1 of this website because it leads the botanical block and because its amount is printed, not because a quarter of a milligram matches a trial.

Guggul

Commiphora mukul, resin50 mg

An Ayurvedic resin with a real randomised record and a disappointing one. The 2003 JAMA trial gave 1,000 to 2,000 mg a day of standardised guggulipid for eight weeks and LDL cholesterol did not fall; a later randomised study reached the same conclusion. At 50 mg this row is a twentieth of those amounts. It is included, and it is not dosed to the research.

Bitter Melon Extract

Momordica charantia L., fruit20 mg

Studied for blood sugar rather than for body weight. A 2019 meta-analysis found a small reduction in fasting glycaemia; the Cochrane review concluded there was not enough evidence to recommend it. Trials generally used around 2,000 mg a day, a hundred times this row.

Licorice Extract

Glycyrrhiza glabra, root25 mg

The row where a small amount is the correct decision rather than a shortfall. The 2023 review of liquorice toxicity collects the reports of raised blood pressure, low potassium and fluid retention, and they attach to sustained intakes near 100 mg a day of glycyrrhizin. Twenty-five milligrams of extract is well under that. Anyone already taking licorice separately, or eating a lot of real liquorice, should add the two together rather than assume they are independent.

Cinnamon Powder

Cinnamomum zeylanicum, bark50 mg

Powder, not extract, which changes the arithmetic. An umbrella meta-analysis of the obesity outcomes and an earlier review of the diabetes ones both pooled trials dosing one to six grams a day. Fifty milligrams is between a twentieth and a hundredth of that. The species is worth noting too: this is Cinnamomum zeylanicum, which carries far less coumarin than the cassia most supermarket cinnamon is.

Gymnema Extract

Gymnema sylvestre, leaf3 mg

Three milligrams. The meta-analysis of glycaemic control and a later review covering body measurements both pooled trials using 200 to 400 mg a day of leaf extract, so this row is around one per cent of the studied amount. Gymnema is the plant behind the sweet-taste suppression effect that makes this category interesting, and that effect comes from holding the leaf in the mouth rather than swallowing a capsule.

Yarrow Powder

Achillea millefolium, flower25 mg

A traditional bitter with no human trial for body weight at all. The current pharmacology review covers mechanism, drug interactions and tolerability rather than outcomes, and it is the honest source to point at. Twenty-five milligrams of flower powder is a culinary amount.

Cayenne Pepper Powder

Capsicum annuum L., fruit, 20M HU/G10 mg

The row most likely to be felt, and the hardest to compare. A meta-analysis of human capsaicin studies and a systematic review of capsaicinoids both measured amounts of capsaicinoids, generally two to ten milligrams, not amounts of powder. Ten milligrams of pepper powder carries a fraction of a milligram of them.

Juniper Extract

Juniperus communis, berry13 mg

Traditional, aromatic, and without a human weight trial. A 2024 review of its constituents is chemistry and lead-compound work rather than clinical outcomes. Thirteen milligrams is included for the same reason juniper appears in gin: it is a familiar bitter botanical.

White Mulberry Extract

Morus alba, leaf3 mg

The second three-milligram row. Mulberry leaf is genuinely interesting because of 1-deoxynojirimycin, which slows starch digestion, and the 2007 human study used 0.8 to 1.2 g of enriched powder per dose. A later dose-finding trial went higher still. Three milligrams of extract is not in that conversation.

Vanadium

as vanadyl sulfate2 mg

A trace mineral with no established Daily Value. The systematic review of oral vanadium found the trials used 50 to 300 mg a day of vanadyl sulfate, reported gastrointestinal side effects at those amounts, and judged the evidence insufficient. Two milligrams is far below all of it, which on this row is the conservative and correct decision rather than a gap.

Alpha Lipoic Acid

30 mg

One of two free compounds on the panel. A 2017 meta-analysis of randomised trials pooled doses of 300 to 1,800 mg a day and found an average difference of about 1.3 kg. Thirty milligrams is a tenth of the smallest of those. It is a real antioxidant at a nutritional amount rather than a therapeutic one.

L-Taurine

25 mg

The other free compound. A 2024 meta-analysis in adults with overweight or obesity pooled supplementation at 1.5 to 6 g a day. Twenty-five milligrams is roughly a hundredth of that, and less than a cup of tea contributes on its own.

Magnesium

as magnesium oxide125 mg

Thirty per cent of the Daily Value, which is a genuine nutritional contribution, in the salt with the poorest absorption record of the common ones. A controlled comparison against magnesium diglycinate is the usual citation for that, and the NIH fact sheet covers what magnesium is for. What is not absorbed stays in the gut, which is why this is the row most likely to be noticed in the first week.

Zinc

as zinc oxide8 mg

Seventy-three per cent of the Daily Value, a sensible daily amount. The dose-response meta-analysis on body weight used 20 to 100 mg, so this row is nutrition rather than intervention. The NIH fact sheet is worth reading before stacking it with a multivitamin, because zinc and copper compete.

Biotin

300 mcg

Ten times the adequate intake for an adult, and the row with the only consequence that shows up inside a week. It is not a safety problem. At supplemental amounts biotin distorts several common immunoassays, including some thyroid and cardiac markers, and the FDA published a safety communication about exactly that. The reading moves, not the patient. Mention it before blood is drawn.

Vitamin C

as ascorbic acid50 mg

Fifty-six per cent of the Daily Value. A 2024 review of vitamin C requirements and body size is the relevant reading: requirements appear to rise with body mass, which makes an ordinary amount here reasonable rather than decorative.

Vitamin E

as DL-alpha tocopheryl acetate7 mg

Forty-seven per cent of the Daily Value, in the synthetic form. The NIH fact sheet covers the difference between the natural and synthetic forms and the upper intake level, which this amount is nowhere near.

Manganese

as manganese amino acid chelate1 mg

Forty-three per cent of the Daily Value, and the quietest row on the panel. The NIH fact sheet sets out what manganese does and where the intake ceiling sits. One milligram is an ordinary supplemental amount.

The absences that matter

What is not in Evo Slim

Five things worth confirming, because a photograph cannot show any of them.

  • No caffeine, and no other stimulant.
  • No proprietary blend, and no unlabelled amount.
  • No gelatin in the capsule shell. It is hypromellose.
  • No prescription ingredient. This is a dietary supplement, and the claims a supplement label may make are structure-and-function statements rather than drug claims.
  • No trial of the finished twenty-row capsule. None is claimed anywhere on this website.
Questions

Evo Slim ingredients: common questions

Does Evo Slim use a proprietary blend?

No. Every one of the twenty rows carries its own milligram or microgram figure. That is the single strongest thing about this label.

Which ingredient is the formula built around?

Chromium, by declared Daily Value. It is the highest figure on the panel at 191% and the row with the most weight research attached to it.

Are any of the amounts large enough to match the trials?

The vitamin and mineral rows are ordinary nutritional amounts and behave like them. Most botanical rows are well below the amounts their published trials used, and the table above prints both figures side by side.

Is there caffeine in it?

No. Nothing on the panel is a stimulant, which is why nothing is felt on day one. Cayenne at 10 mg is the only warming ingredient and it is a small amount.

What are the inactive ingredients?

Hypromellose, which is the capsule shell, and rice flour. Nothing else is listed.

About this review

Sources for the Evo Slim ingredient page

Every study named above, in panel order.

  1. Onakpoya I, Posadzki P, Ernst E. Chromium supplementation in overweight and obesity: a systematic review and meta-analysis of randomized clinical trials. Obes Rev. 2013;14(6):496-507. PMID 23495911. https://pubmed.ncbi.nlm.nih.gov/23495911/
  2. Tian H, Guo X, Wang X, et al. Chromium picolinate supplementation for overweight or obese adults. Cochrane Database Syst Rev. 2013;2013(11):CD010063. PMID 24293292. https://pubmed.ncbi.nlm.nih.gov/24293292/
  3. Docherty JP, Sack DA, Roffman M, et al. A double-blind, placebo-controlled, exploratory trial of chromium picolinate in atypical depression: effect on carbohydrate craving. J Psychiatr Pract. 2005;11(5):302-14. PMID 16184071. https://pubmed.ncbi.nlm.nih.gov/16184071/
  4. Chromium: Fact Sheet for Health Professionals. Office of Dietary Supplements, National Institutes of Health. https://ods.od.nih.gov/factsheets/Chromium-HealthProfessional/
  5. Stohs SJ, Miller H, Kaats GR. A review of the efficacy and safety of banaba (Lagerstroemia speciosa L.) and corosolic acid. Phytother Res. 2012;26(3):317-24. PMID 22095937. https://pubmed.ncbi.nlm.nih.gov/22095937/
  6. Szapary PO, Wolfe ML, Bloedon LT, et al. Guggulipid for the treatment of hypercholesterolemia: a randomized controlled trial. JAMA. 2003;290(6):765-72. PMID 12915429. https://pubmed.ncbi.nlm.nih.gov/12915429/
  7. Nohr LA, Rasmussen LB, Straand J. Resin from the mukul myrrh tree, guggul, can it be used for treating hypercholesterolemia? A randomized, controlled study. Complement Ther Med. 2009;17(1):16-22. PMID 19114224. https://pubmed.ncbi.nlm.nih.gov/19114224/
  8. Peter EL, Kasali FM, Deyno S, et al. Momordica charantia L. lowers elevated glycaemia in type 2 diabetes mellitus patients: Systematic review and meta-analysis. J Ethnopharmacol. 2019;231:311-324. PMID 30385422. https://pubmed.ncbi.nlm.nih.gov/30385422/
  9. Ooi CP, Yassin Z, Hamid TA. Momordica charantia for type 2 diabetes mellitus. Cochrane Database Syst Rev. 2012;2012(8):CD007845. PMID 22895968. https://pubmed.ncbi.nlm.nih.gov/22895968/
  10. Ceccuzzi G, Rapino A, Perna B, et al. Liquorice Toxicity: A Comprehensive Narrative Review. Nutrients. 2023;15(18):3866. PMID 37764649. https://pubmed.ncbi.nlm.nih.gov/37764649/
  11. Keramati M, Musazadeh V, Malekahmadi M, et al. Cinnamon, an effective anti-obesity agent: Evidence from an umbrella meta-analysis. J Food Biochem. 2022;46(8):e14166. PMID 35365881. https://pubmed.ncbi.nlm.nih.gov/35365881/
  12. Allen RW, Schwartzman E, Baker WL, et al. Cinnamon use in type 2 diabetes: an updated systematic review and meta-analysis. Ann Fam Med. 2013;11(5):452-9. PMID 24019277. https://pubmed.ncbi.nlm.nih.gov/24019277/
  13. Devangan S, Varghese B, Johny E, et al. The effect of Gymnema sylvestre supplementation on glycemic control in type 2 diabetes patients: A systematic review and meta-analysis. Phytother Res. 2021;35(12):6802-6812. PMID 34467577. https://pubmed.ncbi.nlm.nih.gov/34467577/
  14. Zamani M, Ashtary-Larky D, Nosratabadi S, et al. The effects of Gymnema Sylvestre supplementation on lipid profile, glycemic control, blood pressure, and anthropometric indices in adults: A systematic review and meta-analysis. Phytother Res. 2023;37(3):949-964. PMID 36580574. https://pubmed.ncbi.nlm.nih.gov/36580574/
  15. Farasati Far B, Behzad G, Khalili H. Achillea millefolium: Mechanism of action, pharmacokinetic, clinical drug-drug interactions and tolerability. Heliyon. 2023;9(12):e22841. PMID 38076118. https://pubmed.ncbi.nlm.nih.gov/38076118/
  16. Zsiboras C, Matics R, Hegyi P, et al. Capsaicin and capsiate could be appropriate agents for treatment of obesity: A meta-analysis of human studies. Crit Rev Food Sci Nutr. 2018;58(9):1419-1427. PMID 28001433. https://pubmed.ncbi.nlm.nih.gov/28001433/
  17. Whiting S, Derbyshire E, Tiwari BK. Capsaicinoids and capsinoids. A potential role for weight management? A systematic review of the evidence. Appetite. 2012;59(2):341-8. PMID 22634197. https://pubmed.ncbi.nlm.nih.gov/22634197/
  18. Jojic AA, Liga S, Utu D, et al. Beyond Essential Oils: Diterpenes, Lignans, and Biflavonoids from Juniperus communis L. as a Source of Multi-Target Lead Compounds. Plants (Basel). 2024;13(22):3233. PMID 39599442. https://pubmed.ncbi.nlm.nih.gov/39599442/
  19. Kimura T, Nakagawa K, Kubota H, et al. Food-grade mulberry powder enriched with 1-deoxynojirimycin suppresses the elevation of postprandial blood glucose in humans. J Agric Food Chem. 2007;55(14):5869-74. PMID 17555327. https://pubmed.ncbi.nlm.nih.gov/17555327/
  20. Thaipitakwong T, Supasyndh O, Rasmi Y, et al. A randomized controlled study of dose-finding, efficacy, and safety of mulberry leaves on glycemic profiles in obese persons with borderline diabetes. Complement Ther Med. 2020;49:102292. PMID 32147046. https://pubmed.ncbi.nlm.nih.gov/32147046/
  21. Smith DM, Pickering RM, Lewith GT. A systematic review of vanadium oral supplements for glycaemic control in type 2 diabetes mellitus. QJM. 2008;101(5):351-8. PMID 18319296. https://pubmed.ncbi.nlm.nih.gov/18319296/
  22. Kucukgoncu S, Zhou E, Lucas KB, et al. Alpha-lipoic acid (ALA) as a supplementation for weight loss: results from a meta-analysis of randomized controlled trials. Obes Rev. 2017;18(5):594-601. PMID 28295905. https://pubmed.ncbi.nlm.nih.gov/28295905/
  23. Sun Q, Wang J, Wang H, et al. Effect of Long-Term Taurine Supplementation on the Lipid and Glycaemic Profile in Adults with Overweight or Obesity: A Systematic Review and Meta-Analysis. Nutrients. 2024;17(1):53. PMID 39796489. https://pubmed.ncbi.nlm.nih.gov/39796489/
  24. Schuette SA, Lashner BA, Janghorbani M. Bioavailability of magnesium diglycinate vs magnesium oxide in patients with ileal resection. JPEN J Parenter Enteral Nutr. 1994;18(5):430-5. PMID 7815675. https://pubmed.ncbi.nlm.nih.gov/7815675/
  25. Magnesium: Fact Sheet for Health Professionals. Office of Dietary Supplements, National Institutes of Health. https://ods.od.nih.gov/factsheets/Magnesium-HealthProfessional/
  26. Abdollahi S, Toupchian O, Jayedi A, et al. Zinc Supplementation and Body Weight: A Systematic Review and Dose-Response Meta-analysis of Randomized Controlled Trials. Adv Nutr. 2020;11(2):398-411. PMID 31504083. https://pubmed.ncbi.nlm.nih.gov/31504083/
  27. Zinc: Fact Sheet for Health Professionals. Office of Dietary Supplements, National Institutes of Health. https://ods.od.nih.gov/factsheets/Zinc-HealthProfessional/
  28. Colon PJ, Greene DN. Biotin Interference in Clinical Immunoassays. J Appl Lab Med. 2018;2(6):941-951. PMID 33636825. https://pubmed.ncbi.nlm.nih.gov/33636825/
  29. Biotin (Vitamin B7): Safety Communication - May Interfere with Lab Tests. U.S. Food and Drug Administration. https://www.fda.gov/medical-devices/safety-communications/update-fda-warns-biotin-may-interfere-lab-tests-fda-safety-communication
  30. Bird JK, Feskens EJ, Melse-Boonstra A. A Systematized Review of the Relationship Between Obesity and Vitamin C Requirements. Curr Dev Nutr. 2024;8(5):102152. PMID 38666038. https://pubmed.ncbi.nlm.nih.gov/38666038/
  31. Vitamin E: Fact Sheet for Health Professionals. Office of Dietary Supplements, National Institutes of Health. https://ods.od.nih.gov/factsheets/VitaminE-HealthProfessional/
  32. Manganese: Fact Sheet for Health Professionals. Office of Dietary Supplements, National Institutes of Health. https://ods.od.nih.gov/factsheets/Manganese-HealthProfessional/
  33. Structure/Function Claims. U.S. Food and Drug Administration, Dietary Supplement Labeling Guide. https://www.fda.gov/food/dietary-supplements-guidance-documents-regulatory-information/structurefunction-claims
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Twenty actives, twenty printed amounts, one capsule a day. The packs and the shipping line are on the pricing page.

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