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Ingredients

Slim Metrix Ingredients: All Ten, and the Dose Each One’s Research Used

Slim Metrix carries ten ingredients in the seller’s published list. Chromium as chromium picolinate is 50 mcg and zinc as zinc gluconate is 5.5 mg. Green tea extract and berberine carry standardisations, 50% EGCG and 97%. Six more share a 276 mg blend: resveratrol, milk thistle, cayenne, Korean ginseng, banaba and alpha lipoic acid.

Every ingredient below carries the amount its own published research used, so the two columns can be read against each other rather than one standing in for the other.

Reading the list

How Slim Metrix discloses, and why it takes three tables

RegisterWhich ingredientsWhat a reader can do with it
A printed amountChromium 50 mcg, zinc 5.5 mgCompare it directly against the doses in the trials
A standardisationGreen tea extract 50% EGCG, berberine 97%Judge the quality of the material. The quantity needs a weight
A shared totalThe six inside the 276 mg blendWork out the ceiling. Even division gives 46 mg each

Compiled from the seller’s published ingredient list and the two listing graphics the seller supplies.

Most labels in this category pick one of those three and stay there. This one uses all three at once, which is why a reader who sees two real figures at the top of the list can reasonably assume the rest are similarly specified.

The rest of this page works through the ten in the seller’s own order. Where the label gives a figure, the comparison is exact. Where it gives a percentage or a share, the research column is context and is labelled as context in the card.

Ingredient by ingredient

The ten Slim Metrix ingredients in detail

Chromium

as chromium picolinate50 mcg

The one ingredient on this label where a reader can do the whole comparison without leaving the page. Chromium picolinate is the most-studied form of the mineral, and the question it has been asked for thirty years is whether it helps with body weight and glucose handling.

The answer from the 2013 Cochrane review of chromium picolinate is a qualified no. Pooling doses of 200, 400, 500 and 1,000 mcg a day it found a mean difference of 1.1 kg after 12 to 16 weeks, which its own authors described as of debatable clinical relevance, on low-quality evidence. a 2013 meta-analysis in Obesity Reviews reached a similar place, and a 2019 meta-analysis in Clinical Obesity looked at anthropometric measures specifically, and a 2024 dose-response meta-analysis of chromium and body composition ran the dose-response version of the same question in people with type 2 diabetes.

On glucose, a 2011 trial in Endocrine Practice ran 500 mcg and 1,000 mcg daily in people at risk of diabetes and neither arm separated from placebo on the primary measures. a 2017 pilot trial in the Journal of Dietary Supplements used 1,000 mcg and 600 mcg arms in a pilot. Against all of that, 50 mcg is a nutritional amount rather than a trial amount, and it is worth reading as a mineral top-up in the formula rather than as the active lever.

Zinc

as zinc gluconate5.5 mg

The second printed figure, and a sensible one. Zinc gluconate is a common, well-absorbed form, and 5.5 mg is roughly half an adult daily requirement, which makes it a top-up rather than an intervention.

The glycaemic literature is larger than most people expect. a 2019 meta-analysis in the American Journal of Clinical Nutrition pooled 32 placebo-controlled interventions across 1,700 participants and found consistent reductions in fasting glucose, post-prandial glucose and glycated haemoglobin. a 2013 meta-analysis of zinc and glycaemic control and a 2024 dose-response meta-analysis of zinc supplementation cover the same ground with different methods.

The dose most relevant as a comparison is the 30 mg a day used for 14 weeks in a 2003 controlled trial of low-level zinc supplementation, chosen because it sits under the US upper intake level of 40 mg. That trial matters for a second reason: high supplemental zinc interferes with copper, which a 1990 review of zinc toxicity in the American Journal of Clinical Nutrition documents at 100 to 300 mg a day and a 2001 metabolic-unit study of zinc and copper examines at the other end of the range. At 5.5 mg none of that is in play, which is exactly why this is a reasonable amount to put in a daily capsule.

Green Tea Extract

Camellia sinensis, leaf50% EGCG, 80% catechins

A standardisation without a weight beside it. The percentages describe the material precisely: half of it is epigallocatechin gallate and four fifths of it is catechins of one kind or another. What a capsule contains depends on how many milligrams of that material go in, which is the seller’s to state.

The comparison figures are clear enough. a 2017 meta-analysis of EGCG and energy expenditure reviewed the energy-expenditure work and put a measurable change around 300 mg of EGCG. a 2007 catechin trial in Obesity ran 583 mg of catechins a day against a 96 mg control for twelve weeks and reported a reduction in body fat. a 2016 randomised trial in Clinical Nutrition went to 856.8 mg of EGCG daily in women with central obesity and measured weight and waist changes over the same span.

The sober counterweight is the 2012 Cochrane review of green tea for weight loss, whose pooled estimate across the green tea weight-loss trials was small and not clinically important. The honest summary is that green tea catechins do something measurable to energy expenditure at doses in the hundreds of milligrams, and that what it adds up to over months is modest.

Berberine

Berberis aristata, root and bark97%

The most pharmacologically active name on this label, and the one that most deserves a conversation with a clinician before the first capsule.

Its metabolic evidence is genuinely strong for a botanical. a 2021 meta-analysis of berberine in type 2 diabetes pooled randomised trials in type 2 diabetes and found improvements across the glycaemic measures; a 2015 meta-analysis in the Journal of Ethnopharmacology covered diabetes, lipids and blood pressure together; a 2018 meta-analysis of berberine and blood lipids looked at dyslipidaemia specifically. a 2020 systematic review of berberine and body weight is the systematic review that addresses body weight directly.

Dose is where the comparison bites. a 2024 meta-analysis that records the doses berberine trials use records the commonest regimen across the trials as 0.9 to 1.5 grams a day, usually split across meals because of how berberine behaves in the gut. A once-daily capsule carrying an unstated weight of 97% material is a different proposition from that, and the 97% describes purity rather than quantity.

Berberine is also the ingredient here most likely to interact with a prescription, because it affects the pathways that clear many common drugs and lowers blood glucose in its own right. a 2019 meta-analysis of the berberine and silymarin pairing and a 2022 meta-analysis of berberine with silymarin on liver enzymes cover the berberine and silymarin pairing, which this formula happens to contain.

Resveratrol

inside the 276 mg blendshare not stated

The first of the six blend members, and the one where the blend ceiling is least damaging. a 2019 dose-response meta-analysis in Obesity Reviews ran a dose-response meta-analysis across the obesity measures and found its signal on weight and BMI specifically in trials dosing under 500 mg a day and running three months or longer.

That matters because a share of 276 mg is not automatically outside the studied range, which is unusual among blend ingredients. a 2014 meta-analysis of eleven resveratrol trials pooled eleven randomised trials on glucose control and a 2021 umbrella review of resveratrol meta-analyses is the umbrella review across the metabolic conditions.

The catch is absorption. a 2011 review of resveratrol bioavailability sets out why resveratrol reaches the bloodstream in such small proportions that oral dosing is an inefficient way to deliver it, and a 2020 review of resveratrol's adverse effects reviews what happens at the upper end. A modest share of a blend is a modest intervention.

Milk Thistle

Silybum marianum, 80% silymarininside the blend

Standardised to 80% silymarin, which is the conventional specification, and then placed inside a total that six ingredients share.

The glycaemic trials used far more. a 2006 randomised trial in Phytotherapy Research gave 200 mg three times a day, 600 mg in total, for four months; a 2018 triple-blinded trial in Phytomedicine used 140 mg three times a day, 420 mg in total, for 45 days. Both reported improvements in glycaemic indices in people with type 2 diabetes.

The ceiling case is the 2012 SyNCH trial in JAMA, the JAMA trial that ran 420 mg and 700 mg three times daily for 24 weeks in chronic hepatitis C and found that neither higher-than-customary dose beat placebo on liver enzymes. a 2017 review of silybin chemistry and bioavailability explains the absorption problem underneath all of it. A share of 276 mg is an order of magnitude below any of those numbers.

Cayenne

Capsicum annuum, fruitinside the blend

The appetite ingredient, and the one with the most specific human dose attached to it. a 2014 crossover trial in Appetite gave capsaicin 2.56 mg with every meal, which is about a gram of red chilli pepper, and measured a rise in the sensation of fullness in energy balance and a fall in the desire to eat after dinner in negative energy balance.

a 2018 meta-analysis of capsaicin and capsiate in human studies pooled the human studies of capsaicin and its non-pungent analogues and found effects on energy expenditure and respiratory quotient that the authors considered supportive.

Two things follow. The trial dose is small, which means a share of a 276 mg blend could plausibly reach it. And the trial dose was given with every meal rather than once in the morning, which a single daily capsule cannot reproduce.

Korean Ginseng

Panax ginseng, 8% ginsenosidesinside the blend

Standardised to 8% ginsenosides, which is a respectable specification for the material. a 2014 meta-analysis of ginseng and glycaemic control pooled sixteen randomised trials of the genus and found fasting blood glucose fell by 0.31 mmol/L against control, a real but small effect.

a 2013 trial of Korean red ginseng in overweight adults is the trial closest to this product’s audience: six grams a day of Korean red ginseng rootlets for twelve weeks in non-diabetic overweight and obese adults.

Six grams is more than twenty times the entire blend. Whatever ginseng is doing in this capsule, it is not reproducing that trial, and the sensible reading is that it is present as a traditional companion to the other botanicals rather than as an active dose.

Banaba

Lagerstroemia speciosa, 2% corosolic acidinside the blend

Standardised to 2% corosolic acid, the constituent most of the research concerns. a 2012 review of banaba and corosolic acid is the review that covers the field, and it describes work across animal models, human subjects and in vitro systems using water-soluble leaf extracts, corosolic acid-standardised extracts and purified corosolic acid.

The review notes that pure corosolic acid has been reported to lower blood sugar within an hour in human subjects, which is the most concrete human finding in this ingredient’s file.

At 2% standardisation, a share of a 276 mg blend delivers a small quantity of corosolic acid by any division. The honest position is that banaba has a plausible mechanism, a thin human evidence base, and no agreed effective dose to compare a blend share against.

Alpha Lipoic Acid

inside the blendshare not stated

The ingredient that is on one piece of the vendor’s artwork and absent from the other, and which the seller’s own list confirms belongs inside the blend.

a 2017 meta-analysis of alpha-lipoic acid and weight pooled randomised trials of alpha lipoic acid and weight and found small reductions, with meta-regression showing no relationship between dose and the change in BMI or weight. a 2018 systematic review of alpha-lipoic acid in obesity reached comparable conclusions and put the safe intake at up to 1,200 mg a day.

That upper figure is the useful one for a blend comparison. Trials in this ingredient run to four figures in milligrams; a share of 276 mg across six ingredients is two orders of magnitude below the ceiling those reviews describe.

Honest label analysis

Where the two Slim Metrix ingredient graphics disagree

Six on one card, five on the other, ten in the list

The violet listing card names six ingredients and its footer strip counts them for you. The dark card names five and includes alpha lipoic acid, which the violet card leaves out entirely. The seller’s published list resolves it: alpha lipoic acid is real and sits inside the blend with cayenne, Korean ginseng and banaba, so the six-ingredient card is the incomplete one.

This is the one internal conflict in the material the vendor supplied, and it is worth being precise about what it does and does not mean. It is not evidence of anything being hidden: the fuller list is the one the seller publishes, and it is more generous than the artwork, not less.

It does mean that a buyer who reads only the bottle graphic will believe the formula has six ingredients when it has ten, and four of the four they have not seen are inside a blend whose split is a single number. That is the fact this website exists to put in front of them, and it is stated here once rather than repeated on every page.

What the blend total bounds

The Slim Metrix blend arithmetic

If the 276 mg divides...Each ingredient getsHow that reads
Evenly, six ways46 mgBelow every trial dose on this page that has one
Weighted toward resveratrolup to a few hundred mgOnly possible if the other five are trace amounts
Weighted toward cayennea few milligrams would sufficeThe one ingredient whose trial dose a blend share can reach
Any division at all276 mg is the ceiling for all sixThis is the only statement the figure supports on its own

Arithmetic on the published blend total. The seller has not released the split, so none of the first three rows is a claim about this product.

The fourth row is the one that holds. A blend total is a ceiling, and a ceiling is genuinely informative even when the split is unknown: it rules out the possibility that all six are at trial doses, because six trial doses from this page would run to several grams.

What it cannot do is tell you which of the six were prioritised. A formulator who put most of the 276 mg into resveratrol and cayenne would have built a defensible capsule. One who spread it evenly would have built six trace amounts. The figure is compatible with both, and that is the whole limitation.

What is not here

What is absent from Slim Metrix, and why that is a feature

No caffeine anhydrous. No green coffee bean extract, no raspberry ketone, no garcinia. The four stimulant and thermogenic names that appear in most of this category are all missing from the list, and green tea extract is the only ingredient here that touches that territory at all.

That is a deliberate formulation choice and it has consequences in both directions. It removes the jitter, the effect on sleep, the interaction with the coffee already in the morning, and the whole class of cardiovascular cautions that come with a stimulant blend. It is the reason the label can claim steady energy without a crash and mean something specific by it.

It also removes the one ingredient class in this category that reliably produces a same-day sensation. A buyer who has taken a stimulant-based product before will find this one quiet, and the results timeline is the page that sets expectations for what that quiet means.

About this review

Sources for the Slim Metrix ingredient doses

  1. Tian H, Guo X, Wang X, et al. Chromium picolinate supplementation for overweight or obese adults. Cochrane Database Syst Rev. 2013;2013(11):CD010063. Doses pooled: 200, 400, 500 and 1,000 mcg a day; mean difference -1.1 kg after 12 to 16 weeks, graded low-quality evidence. PMID 24293292. https://pubmed.ncbi.nlm.nih.gov/24293292/
  2. 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/
  3. Tsang C, Taghizadeh M, Aghabagheri E, et al. A meta-analysis of the effect of chromium supplementation on anthropometric indices of subjects with overweight or obesity. Clin Obes. 2019;9(4):e12313. PMID 31115179. https://pubmed.ncbi.nlm.nih.gov/31115179/
  4. Vajdi M, Khajeh M, Safaei E, et al. Effects of chromium supplementation on body composition in patients with type 2 diabetes: A dose-response systematic review and meta-analysis of randomized controlled trials. J Trace Elem Med Biol. 2024;81:127338. PMID 37952433. https://pubmed.ncbi.nlm.nih.gov/37952433/
  5. Sala M, Breithaupt L, Bulik CM, et al. A Double-Blind, Randomized Pilot Trial of Chromium Picolinate for Overweight Individuals with Binge-Eating Disorder: Effects on Glucose Regulation. J Diet Suppl. 2017;14(2):191-199. Arms of 1,000 mcg and 600 mcg a day. PMID 27835050. https://pubmed.ncbi.nlm.nih.gov/27835050/
  6. Suksomboon N, Poolsup N, Yuwanakorn A. Systematic review and meta-analysis of the efficacy and safety of chromium supplementation in diabetes. J Clin Pharm Ther. 2014;39(3):292-306. PMID 24635480. https://pubmed.ncbi.nlm.nih.gov/24635480/
  7. Ali A, Ma Y, Reynolds J, et al. Chromium effects on glucose tolerance and insulin sensitivity in persons at risk for diabetes mellitus. Endocr Pract. 2011;17(1):16-25. Chromium picolinate at 500 mcg or 1,000 mcg a day; neither dose separated from placebo on the primary measures. PMID 20634174. https://pubmed.ncbi.nlm.nih.gov/20634174/
  8. Wang X, Wu W, Zheng W, et al. Zinc supplementation improves glycemic control for diabetes prevention and management: a systematic review and meta-analysis of randomized controlled trials. Am J Clin Nutr. 2019;110(1):76-90. Thirty-two placebo-controlled interventions, 1,700 participants. PMID 31161192. https://pubmed.ncbi.nlm.nih.gov/31161192/
  9. Capdor J, Foster M, Petocz P, et al. Zinc and glycemic control: a meta-analysis of randomised placebo controlled supplementation trials in humans. J Trace Elem Med Biol. 2013;27(2):137-42. PMID 23137858. https://pubmed.ncbi.nlm.nih.gov/23137858/
  10. Nazari M, Nikbaf-Shandiz M, Pashayee-Khamene F, et al. Zinc Supplementation in Individuals with Prediabetes and type 2 Diabetes: a GRADE-Assessed Systematic Review and Dose-Response Meta-analysis. Biol Trace Elem Res. 2024;202(7):2966-2990. PMID 37870684. https://pubmed.ncbi.nlm.nih.gov/37870684/
  11. Bonham M, O'Connor JM, McAnena LB, et al. Zinc supplementation has no effect on lipoprotein metabolism, hemostasis, and putative indices of copper status in healthy men. Biol Trace Elem Res. 2003;93(1-3):75-86. Zinc 30 mg a day for 14 weeks, a total intake of 40 mg a day against the US tolerable upper intake level. PMID 12835492. https://pubmed.ncbi.nlm.nih.gov/12835492/
  12. Fosmire GJ. Zinc toxicity. Am J Clin Nutr. 1990;51(2):225-7. Reports induced copper deficiency at supplemental intakes of 100 to 300 mg a day against a recommended dietary allowance of 15 mg. PMID 2407097. https://pubmed.ncbi.nlm.nih.gov/2407097/
  13. Kapoor MP, Sugita M, Fukuzawa Y, et al. Physiological effects of epigallocatechin-3-gallate (EGCG) on energy expenditure for prospective fat oxidation in humans: A systematic review and meta-analysis. J Nutr Biochem. 2017;43:1-10. The authors place a metabolic-rate signal at a 300 mg EGCG dose. PMID 27883924. https://pubmed.ncbi.nlm.nih.gov/27883924/
  14. Nagao T, Hase T, Tokimitsu I. A green tea extract high in catechins reduces body fat and cardiovascular risks in humans. Obesity (Silver Spring). 2007;15(6):1473-83. 583 mg of catechins a day against a 96 mg control. PMID 17557985. https://pubmed.ncbi.nlm.nih.gov/17557985/
  15. Chen IJ, Liu CY, Chiu JP, et al. Therapeutic effect of high-dose green tea extract on weight reduction: A randomized, double-blind, placebo-controlled clinical trial. Clin Nutr. 2016;35(3):592-9. EGCG 856.8 mg a day for 12 weeks in women with central obesity. PMID 26093535. https://pubmed.ncbi.nlm.nih.gov/26093535/
  16. Jurgens TM, Whelan AM, Killian L, et al. Green tea for weight loss and weight maintenance in overweight or obese adults. Cochrane Database Syst Rev. 2012;12(12):CD008650. PMID 23235664. https://pubmed.ncbi.nlm.nih.gov/23235664/
  17. Guo J, Chen H, Zhang X, et al. The Effect of Berberine on Metabolic Profiles in Type 2 Diabetic Patients: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Oxid Med Cell Longev. 2021;2021:2074610. PMID 34956436. https://pubmed.ncbi.nlm.nih.gov/34956436/
  18. Wang J, Bi C, Xi H, et al. Effects of administering berberine alone or in combination on type 2 diabetes mellitus: a systematic review and meta-analysis. Front Pharmacol. 2024;15:1455534. The commonest dose across the included trials is 0.9 to 1.5 g a day, in courses of one to three months. PMID 39640489. https://pubmed.ncbi.nlm.nih.gov/39640489/
  19. Ilyas Z, Perna S, Al-Thawadi S, et al. The effect of Berberine on weight loss in order to prevent obesity: A systematic review. Biomed Pharmacother. 2020;127:110137. Human work summarised from a 300 mg daily dose upward, with glucose effects reported around 1.0 g. PMID 32353823. https://pubmed.ncbi.nlm.nih.gov/32353823/
  20. Mousavi SM, Milajerdi A, Sheikhi A, et al. Resveratrol supplementation significantly influences obesity measures: a systematic review and dose-response meta-analysis of randomized controlled trials. Obes Rev. 2019;20(3):487-498. The weight and BMI signal sits in trials dosing under 500 mg a day and running three months or longer. PMID 30515938. https://pubmed.ncbi.nlm.nih.gov/30515938/
  21. Walle T. Bioavailability of resveratrol. Ann N Y Acad Sci. 2011;1215:9-15. PMID 21261636. https://pubmed.ncbi.nlm.nih.gov/21261636/
  22. Huseini HF, Larijani B, Heshmat R, et al. The efficacy of Silybum marianum (L.) Gaertn. (silymarin) in the treatment of type II diabetes: a randomized, double-blind, placebo-controlled, clinical trial. Phytother Res. 2006;20(12):1036-9. Silymarin 200 mg three times a day, 600 mg daily, for four months. PMID 17072885. https://pubmed.ncbi.nlm.nih.gov/17072885/
  23. Ebrahimpour-Koujan S, Gargari BP, Mobasseri M, et al. Lower glycemic indices and lipid profile among type 2 diabetes mellitus patients who received novel dose of Silybum marianum (L.) Gaertn. (silymarin) extract supplement: A Triple-blinded randomized controlled clinical trial. Phytomedicine. 2018;44:39-44. Silymarin 140 mg three times a day, 420 mg daily, for 45 days. PMID 29895491. https://pubmed.ncbi.nlm.nih.gov/29895491/
  24. Fried MW, Navarro VJ, Afdhal N, et al. Effect of silymarin (milk thistle) on liver disease in patients with chronic hepatitis C unsuccessfully treated with interferon therapy: a randomized controlled trial. JAMA. 2012;308(3):274-82. Silymarin 420 mg or 700 mg three times a day for 24 weeks; neither arm beat placebo. PMID 22797645. https://pubmed.ncbi.nlm.nih.gov/22797645/
  25. Janssens PL, Hursel R, Westerterp-Plantenga MS. Capsaicin increases sensation of fullness in energy balance, and decreases desire to eat after dinner in negative energy balance. Appetite. 2014;77:44-9. Capsaicin 2.56 mg with every meal, which is 1.03 g of red chilli pepper. PMID 24630935. https://pubmed.ncbi.nlm.nih.gov/24630935/
  26. 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/
  27. Shishtar E, Sievenpiper JL, Djedovic V, et al. The effect of ginseng (the genus panax) on glycemic control: a systematic review and meta-analysis of randomized controlled clinical trials. PLoS One. 2014;9(9):e107391. Sixteen trials; fasting glucose fell by 0.31 mmol/L against control. PMID 25265315. https://pubmed.ncbi.nlm.nih.gov/25265315/
  28. Cho YH, Ahn SC, Lee SY, et al. Effect of Korean red ginseng on insulin sensitivity in non-diabetic healthy overweight and obese adults. Asia Pac J Clin Nutr. 2013;22(3):365-71. Six grams of red ginseng rootlets a day for 12 weeks. PMID 23945406. https://pubmed.ncbi.nlm.nih.gov/23945406/
  29. 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/
  30. 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. Dose showed no relationship with the change in weight or BMI. PMID 28295905. https://pubmed.ncbi.nlm.nih.gov/28295905/
  31. Namazi N, Larijani B, Azadbakht L. Alpha-lipoic acid supplement in obesity treatment: A systematic review and meta-analysis of clinical trials. Clin Nutr. 2018;37(2):419-428. The authors put the safe intake at up to 1,200 mg a day. PMID 28629898. https://pubmed.ncbi.nlm.nih.gov/28629898/
The Slim Metrix three-bottle pack, front labels showing

Order Slim Metrix with the ingredient list in front of you

Ten names, two printed amounts and one blend total. Read the bottle you receive against this page, and use the window if the two do not match.

Two bottles $158 · six bottles $294 · 60-day money-back guarantee

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One capsule a morning · 30 per bottle · lot SLI-26/SL-3249

60-day money-back guarantee

The window is two months. The reported wait is three to six weeks.

Those two numbers leave a fortnight of margin, which is unusual enough in this category to be worth saying out loud. The seller counts the 60 days from the purchase date, return postage is yours, and the desk needs the order ID before it can start anything. The steps are set out on the refund policy page.

Order Slim Metrix On The Official Website

Lot SLI-26/SL-3249 · from $49 a bottle · read the guarantee first

The Slim Metrix six-bottle pack, front labels showing
Slim Metrix · one capsule each morning $49 a bottle on the six-pack · 60-day money-back guarantee
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