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The Detox Pills Formula Explained

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Detox Pills is smööts' liver support formula, made for anyone who wants to support their liver's own natural processes, for example after a period of heavier drinking, richer food, or simply as ongoing daily support. It combines NAC, an amino acid derivative studied as a precursor to the body's main internal antioxidant, silymarin from milk thistle, artichoke and dandelion, two traditional liver-supporting plants, glutathione itself, and Bioperine to support absorption. It is designed to support normal liver function alongside a healthy lifestyle, not to reverse diagnosed liver disease or "detox" the body of anything in a literal sense.

60 vegan capsules per pot, 2 a day = a 30-day supply. Each capsule combines NAC (N-acetylcysteine), Silymarin, Artichoke, Dandelion, Glutathione and Bioperine (black pepper extract).

NAC in Detox Pills

NAC, or N-acetylcysteine, is a modified form of the amino acid cysteine. The body uses cysteine as one of three building blocks to make glutathione, its main internally produced antioxidant, and NAC is the form most reliably absorbed and used for this purpose, which is why it is included here rather than glutathione's other building blocks.

Human trials have mostly studied NAC in people with a diagnosed liver condition, which gives a clearer picture of what it does to liver enzymes than a healthy-population trial would. In a randomised controlled trial in people with non-alcoholic fatty liver disease, three months of oral NAC produced a significantly greater fall in the liver enzyme ALT than vitamin C.[1] A randomised controlled trial in people with cirrhosis found that daily NAC over the study period improved liver enzyme levels (ALT, AST and ALP) and reduced markers used to score liver disease severity, compared with placebo.[2] A three-arm randomised controlled trial in people with non-alcoholic steatohepatitis found NAC was the only one of three treatments tested (alongside rosuvastatin and vitamin E) to produce a significant improvement in liver stiffness, a measure of scarring, over the study period.[3] A more recent randomised controlled trial in people with fatty liver disease found high-dose NAC improved markers of oxidative stress and insulin resistance compared with lifestyle changes alone.[4]

The honest limitation is that these trials were run in people with a diagnosed liver condition and used doses higher than a typical food supplement, so we cannot assume the same size of effect in a healthy person taking NAC as daily support. NAC does not "detox" the liver in any literal sense; its studied role is narrower and more mechanistic, supporting the body's own antioxidant production.

Silymarin in Detox Pills

Silymarin is the group of active compounds extracted from milk thistle (Silybum marianum) seeds, most notably silybin.[5] It has one of the longest research histories of any liver-supporting botanical, studied for its antioxidant properties and its potential to support liver cells under stress.

A meta-analysis of five randomised controlled trials in over a thousand people taking anti-tuberculosis medication (a drug class known to stress the liver) found silymarin significantly reduced the occurrence of drug-induced liver injury and improved liver enzyme levels compared with placebo.[6] A separate meta-analysis of eight randomised controlled trials in people with non-alcoholic fatty liver disease found silymarin produced a greater reduction in AST and ALT than control treatment.[7] However, not every condition shows the same result: a meta-analysis of five randomised trials in people with chronic hepatitis C found oral silymarin's effect on ALT was no different from placebo.[8] The largest and most recent analysis, pooling 55 randomised trials across different liver conditions, found that lower doses (under 400 mg) and shorter courses (up to two months) were associated with better reductions in liver enzymes than higher doses or longer use, and that silymarin worked better in NAFLD and viral hepatitis than in drug- or alcohol-related liver injury.[9]

This is a good example of why we want to avoid blanket claims: silymarin's benefit for liver enzymes depends heavily on which condition is being studied, the dose used and how long it is taken for, and it clearly does not help equally in every situation. We include it on the strength of the more consistently positive NAFLD and drug-induced liver injury evidence.

Artichoke in Detox Pills

Artichoke leaf extract comes from Cynara scolymus, the same plant as the globe artichoke eaten as a vegetable. Its leaves are rich in cynarin and chlorogenic acid, compounds studied for their effects on bile production and liver enzyme levels, and it has a long history of traditional use to support digestion of fats.

A randomised, double-blind, placebo-controlled trial in 60 people with non-alcoholic steatohepatitis found two months of artichoke leaf extract significantly improved ALT and AST levels, alongside reductions in triglycerides and cholesterol, compared with placebo.[10] A pilot, double-blind, randomised controlled trial in 100 people with non-alcoholic fatty liver disease found two months of artichoke leaf extract improved liver enzymes, liver size on ultrasound and total bilirubin compared with placebo.[11] A separate randomised, double-blind, placebo-controlled trial in 80 people with metabolic syndrome found 12 weeks of artichoke leaf extract significantly lowered oxidised LDL, a marker of oxidative damage to cholesterol particles, compared with placebo.[12]

These are genuinely encouraging results, but the trials are relatively small (60 to 100 participants), mostly short (2 to 3 months), and were run in people with a diagnosed liver or metabolic condition rather than healthy adults, so we would not claim the same scale of benefit for someone using it as everyday support rather than treatment.

Dandelion in Detox Pills

Dandelion, from the plant Taraxacum officinale, has one of the longest folk histories of any liver-supporting herb across European and Chinese traditional medicine, historically used to support bile flow and digestion of fats.[13] In Detox Pills it is included largely on the strength of this traditional use and its laboratory pharmacology.

The evidence here is honestly weighted towards animal and laboratory research rather than human trials. In one controlled study, rats given a toxic liver-damaging compound alongside dandelion leaf extract showed better-preserved liver enzyme levels and less tissue damage than rats given the toxin alone.[14] A 2025 review pulling together the available pharmacological literature on dandelion and the liver describes plausible antioxidant and anti-inflammatory mechanisms, largely from cell and animal studies of its bioactive compound taraxasterol, and explicitly notes that clinical trials in humans are still lacking.[15]

We want to be completely transparent about this one: dandelion is the ingredient in this formula with the least direct human clinical evidence behind it. Its inclusion rests on a long history of traditional use and consistent, if preclinical, laboratory pharmacology, not on human liver enzyme trials. If dedicated human trials are published in future, we will update this page.

Glutathione in Detox Pills

Glutathione is a small molecule made from three amino acids, produced naturally in every cell in the body, where it acts as the main internal antioxidant.[16] It is included directly in Detox Pills alongside NAC, its building block, because oral glutathione itself has also been tested as a supplement.

Results for oral glutathione are genuinely mixed, and this is worth stating plainly rather than glossing over. A randomised, double-blind, placebo-controlled trial in healthy adults found no significant change in oxidative stress biomarkers after oral glutathione supplementation.[17] In contrast, a six-month randomised, double-blind, placebo-controlled trial found daily oral glutathione (250 or 1,000 mg) significantly raised glutathione levels in blood, plasma and cells over the study period.[18] In older adults with type 2 diabetes, a randomised clinical trial found six months of oral glutathione reduced a marker of oxidative DNA damage and improved blood sugar control (HbA1c) within three months, with the biggest benefit in those over 55.[19] More recent pharmacokinetic work in a small randomised crossover trial has focused on why some oral glutathione formulations are absorbed better than others, since the molecule is broken down in the gut before much of a standard dose reaches the bloodstream.[20]

The honest picture is that oral glutathione's bioavailability is a genuine, unresolved question in the research, and results vary between trials, possibly because of differences in formulation, dose, duration and how glutathione status was measured. We include it as a complementary source alongside NAC rather than as the sole basis for this formula's claims.

Bioperine in Detox Pills

Bioperine is a patented, standardised extract of black pepper (Piper nigrum) fruit, standardised to a set level of piperine, its main active alkaloid. It is included to support the absorption of the other ingredients in this formula rather than for a liver effect of its own.

Piperine's absorption-enhancing action was first characterised in pharmacokinetic studies showing rapid intestinal uptake and inhibition of enzymes and transporters that would otherwise limit how much of a compound reaches the bloodstream.[21] In a human and animal study, a 20 mg dose of piperine taken alongside curcumin increased peak blood levels of curcumin roughly twentyfold in human volunteers.[22] A separate double-blind, placebo-controlled study in healthy men found that piperine alongside coenzyme Q10 for 21 days produced around 30% greater plasma CoQ10 levels than CoQ10 alone.[23]

These trials tested curcumin and coenzyme Q10 specifically, not NAC, silymarin, artichoke, dandelion or glutathione, so piperine's benefit within Detox Pills is a reasonable, mechanism-based inference rather than something measured directly in this combination. Because piperine can also affect how the liver processes certain medications, anyone on regular prescription medicine should check with a doctor or pharmacist before combining.

How to take

Take 2 capsules a day with water, ideally with a meal. One pot lasts 30 days. Most of the supporting research used daily use for 2 to 6 months, so give the formula time and pair it with a generally healthy diet and moderate alcohol intake rather than expecting it to offset an unhealthy lifestyle.

Ingredients and nutritional information

Each pack contains: 60 capsules · 30 days

Serving: Morning, with water.

Active ingredients: N-Acetyl Cysteine (NAC), Milk thistle extract (80% silymarin), Artichoke leaf extract, Dandelion root extract, Glutathione (reduced), Bioperine (black pepper extract).

Per daily serving% NRV*
N-Acetyl Cysteine (NAC)600 mg†
Milk thistle extract (80% silymarin)250 mg†
Artichoke leaf extract150 mg†
Dandelion root extract100 mg†
Glutathione (reduced)100 mg†
Bioperine (black pepper extract)5 mg†

*NRV: Nutrient Reference Value, Regulation (EU) No 1169/2011. † No NRV established.

Cautions and allergen advice

  • Pregnancy and breastfeeding: Speak to your doctor before use during pregnancy or breastfeeding, as NAC, silymarin, artichoke, dandelion and concentrated glutathione have not been adequately studied at supplement doses in these groups.
  • Medications: NAC may increase the effect of nitroglycerin and other nitrate medications, and can theoretically interact with medications broken down by the liver. Artichoke and dandelion can increase bile flow and should be used with caution alongside medication for gallstones or bile duct problems. Bioperine can increase the absorption of some prescription medications, so check with a pharmacist if you take regular medicine.
  • Children: Not intended for anyone under 18.
  • Medical conditions: Avoid dandelion and artichoke if you have gallstones, bile duct obstruction, or a known allergy to plants in the daisy (Asteraceae/Compositae) family, such as ragweed, marigold or chrysanthemum. Speak to your doctor before use if you have a diagnosed liver condition (such as hepatitis, cirrhosis or fatty liver disease); this formula is designed as everyday support, not as a substitute for medical treatment or monitoring. NAC and asthma medication should be combined only with medical advice, as NAC has occasionally been linked to bronchospasm in sensitive individuals.
  • Food supplements should not be used as a substitute for a varied and balanced diet and a healthy lifestyle. Do not exceed the recommended daily dose.

Allergen advice

Detox Pills is formulated without any of the 14 EU-listed allergens as intentional ingredients: NAC, Silymarin, Artichoke, Dandelion, Glutathione and Bioperine are all plant or amino-acid derived, and the capsule shell is vegan. Anyone with a known allergy to plants in the daisy (Asteraceae/Compositae) family, which artichoke and dandelion both belong to, should check the individual ingredients against their own sensitivities.

Detox Pills is produced in a facility that also handles other food supplement ingredients and follows standard allergen control procedures to minimise the risk of cross-contact. Always read the label before use, particularly if you have a diagnosed food allergy or intolerance.

References

  1. Khoshbaten M, Aliasgarzadeh A, Masnadi K, Tarzamani MK, Farhang S, Babaei H, Kiani J, Zaare M, Najafipoor F. N-acetylcysteine improves liver function in patients with non-alcoholic fatty liver disease. Hepat Mon. 2010 Winter;10(1):12-6. PubMed
  2. Hatami B, Abdi S, Pourhoseingholi MA, Eghlimi H, Rabbani AH, Masoumi M, Hajimohammadebrahim-Ketabforoush M. The effects of N-acetylcysteine on hepatic, hematologic, and renal parameters in cirrhotic patients: a randomized controlled trial. Gastroenterol Hepatol Bed Bench. 2023;16(4):432-440. doi:10.22037/ghfbb.v16i4.2443
  3. Zakaria AY, Badawi R, Osama H, Abdelrahman MA, El-Kalaawy AM. A Comparative Study of N-Acetyl Cysteine, Rosuvastatin, and Vitamin E in the Management of Patients with Non-Alcoholic Steatohepatitis: A Randomized Controlled Trial. Pharmaceuticals (Basel). 2025 Apr 29;18(5). doi:10.3390/ph18050650
  4. Ramadan AM, El-Wakeel LM, Adel A, Abdel-Wahab M, Fahmy SF. Effect of high dose N-acetyl cysteine supplementation on markers of oxidative stress and insulin resistance in non-diabetic patients with metabolic dysfunction associated steatotic liver disease: a randomized controlled trial. BMC Gastroenterol. 2026 Aug 12;26(1). doi:10.1186/s12876-026-05157-x
  5. National Center for Complementary and Integrative Health. (n.d.). Milk Thistle. National Institutes of Health. nccih.nih.gov
  6. Tao L, Qu X, Zhang Y, Song Y, Zhang SX. Prophylactic Therapy of Silymarin (Milk Thistle) on Antituberculosis Drug-Induced Liver Injury: A Meta-Analysis of Randomized Controlled Trials. Can J Gastroenterol Hepatol. 2019;2019:3192351. doi:10.1155/2019/3192351
  7. Zhong S, Fan Y, Yan Q, Fan X, Wu B, Han Y, Zhang Y, Chen Y, Zhang H, Niu J. The therapeutic effect of silymarin in the treatment of nonalcoholic fatty disease: A meta-analysis (PRISMA) of randomized control trials. Medicine (Baltimore). 2017 Dec;96(49):e9061. doi:10.1097/MD.0000000000009061
  8. Yang Z, Zhuang L, Lu Y, Xu Q, Chen X. Effects and tolerance of silymarin (milk thistle) in chronic hepatitis C virus infection patients: a meta-analysis of randomized controlled trials. Biomed Res Int. 2014;2014:941085. doi:10.1155/2014/941085
  9. Shahsavari K, Ardekani SS, Ardekani MRS, Esfahani MM, Kazemizadeh H, Jamialahmadi T, Iranshahi M, Khanavi M, Hasanpour M. Are alterations needed in Silybum marianum (Silymarin) administration practices? A novel outlook and meta-analysis on randomized trials targeting liver injury. BMC Complement Med Ther. 2025 Apr 12;25(1):134. doi:10.1186/s12906-025-04886-y
  10. Rangboo V, Noroozi M, Zavoshy R, Rezadoost SA, Mohammadpoorasl A. The Effect of Artichoke Leaf Extract on Alanine Aminotransferase and Aspartate Aminotransferase in the Patients with Nonalcoholic Steatohepatitis. Int J Hepatol. 2016;2016:4030476. doi:10.1155/2016/4030476
  11. Panahi Y, Kianpour P, Mohtashami R, Atkin SL, Butler AE, Jafari R, Badeli R, Sahebkar A. Efficacy of artichoke leaf extract in non-alcoholic fatty liver disease: A pilot double-blind randomized controlled trial. Phytother Res. 2018 Jul;32(7):1382-1387. doi:10.1002/ptr.6073
  12. Rezazadeh K, Aliashrafi S, Asghari-Jafarabadi M, Ebrahimi-Mameghani M. Antioxidant response to artichoke leaf extract supplementation in metabolic syndrome: A double-blind placebo-controlled randomized clinical trial. Clin Nutr. 2018 Jun;37(3):790-796. doi:10.1016/j.clnu.2017.03.017
  13. National Center for Complementary and Integrative Health. (n.d.). Dandelion. National Institutes of Health. nccih.nih.gov
  14. Hfaiedh M, Brahmi D, Zourgui L. Hepatoprotective effect of Taraxacum officinale leaf extract on sodium dichromate-induced liver injury in rats. Environ Toxicol. 2016 Mar;31(3):339-49. doi:10.1002/tox.22048
  15. Herrera Vielma F, Quiñones San Martin M, Muñoz-Carrasco N, Berrocal-Navarrete F, González DR, Zúñiga-Hernández J. The Role of Dandelion (Taraxacum officinale) in Liver Health and Hepatoprotective Properties. Pharmaceuticals (Basel). 2025 Jul 1;18(7). doi:10.3390/ph18070990
  16. National Center for Complementary and Integrative Health. (n.d.). Antioxidants: In Depth. National Institutes of Health. nccih.nih.gov
  17. Allen J, Bradley RD. Effects of oral glutathione supplementation on systemic oxidative stress biomarkers in human volunteers. J Altern Complement Med. 2011 Sep;17(9):827-33. doi:10.1089/acm.2010.0716
  18. Richie JP Jr, Nichenametla S, Neidig W, Calcagnotto A, Haley JS, Schell TD, Muscat JE. Randomized controlled trial of oral glutathione supplementation on body stores of glutathione. Eur J Nutr. 2015 Mar;54(2):251-63. doi:10.1007/s00394-014-0706-z
  19. Kalamkar S, Acharya J, Kolappurath Madathil A, Gajjar V, Divate U, Karandikar-Iyer S, Goel P, Ghaskadbi S. Randomized Clinical Trial of How Long-Term Glutathione Supplementation Offers Protection from Oxidative Damage and Improves HbA1c in Elderly Type 2 Diabetic Patients. Antioxidants (Basel). 2022 May 23;11(5). doi:10.3390/antiox11051026
  20. Solnier J, Du M, Zhang Y, Roh YS, Kuo YC, Ibi A, Wood S, Hardy M, Gahler RJ, Chang C. A Targeted Metabolomic Assessment of Oral Glutathione Bioavailability and Safety in Humans: A Randomized Crossover Clinical Trial. Antioxidants (Basel). 2026 Mar 11;15(3). doi:10.3390/antiox15030354
  21. Khajuria A, Zutshi U, Bedi KL. Permeability characteristics of piperine on oral absorption--an active alkaloid from peppers and a bioavailability enhancer. Indian J Exp Biol. 1998 Jan;36(1):46-50. PubMed
  22. Shoba G, Joy D, Joseph T, Majeed M, Rajendran R, Srinivas PS. Influence of piperine on the pharmacokinetics of curcumin in animals and human volunteers. Planta Med. 1998 May;64(4):353-6. doi:10.1055/s-2006-957450
  23. Badmaev V, Majeed M, Prakash L. Piperine derived from black pepper increases the plasma levels of coenzyme Q10 following oral supplementation. J Nutr Biochem. 2000 Feb;11(2):109-13. doi:10.1016/s0955-2863(99)00074-1
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