Dandelion Root Extract is a traditional herbal remedy rich in bitter compounds and prebiotic inulin that supports liver detoxification, digestive health, and healthy inflammatory response while providing gentle diuretic effects.
Alternative Names: Taraxacum officinale Root Extract, Lion’s Tooth Root Extract, Blowball Root Extract, Wild Endive Root Extract, Priest’s Crown Root Extract
Categories: Herbal Extract, Botanical, Bitter Herb
Primary Longevity Benefits
- Liver support
- Digestive health
- Anti-inflammatory
- Antioxidant
Secondary Benefits
- Diuretic effect
- Blood sugar regulation
- Prebiotic activity
- Bile flow stimulation
- Mild laxative
- Potential anti-cancer properties
Mechanism of Action
Dandelion root extract (Taraxacum officinale) exerts its biological effects through multiple mechanisms involving a diverse array of bioactive compounds. The primary active constituents include sesquiterpene lactones (particularly taraxacin and taraxinic acid), triterpenes (taraxasterol, taraxerol), phenolic compounds (chicoric acid, chlorogenic acid, caffeic acid), polysaccharides (particularly inulin), and various minerals. One of the most well-established mechanisms is hepatoprotective activity. Dandelion root extract enhances liver detoxification pathways, particularly Phase II detoxification enzymes such as glutathione S-transferase, which conjugate toxins for elimination.
It also increases the production and flow of bile, a process known as choleretic activity, which is mediated primarily by sesquiterpene lactones and bitter compounds stimulating bile production in the liver and bile release from the gallbladder. This enhanced bile flow supports digestion and helps eliminate waste products processed by the liver. The extract’s anti-inflammatory properties are mediated through multiple pathways. It inhibits nuclear factor-kappa B (NF-κB) activation, a master regulator of inflammatory responses, thereby reducing the production of pro-inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α), interleukin-1β (IL-1β), and interleukin-6 (IL-6).
Dandelion root compounds, particularly phenolic acids, also inhibit cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS), further contributing to its anti-inflammatory effects. The antioxidant activity of dandelion root extract is attributed to its rich content of phenolic compounds, which directly scavenge free radicals and reactive oxygen species. Additionally, it enhances endogenous antioxidant defenses by increasing the activity of superoxide dismutase (SOD), catalase, and glutathione peroxidase enzymes. This dual mechanism provides comprehensive protection against oxidative stress.
Dandelion root’s diuretic effect, which gives the plant its French name ‘pissenlit’ (wet the bed), is primarily due to its high potassium content and the presence of sesquiterpene lactones. Unlike pharmaceutical diuretics, dandelion root increases urine output without depleting potassium, making it a gentler alternative for promoting fluid balance. The extract’s effects on blood glucose regulation involve multiple mechanisms. It inhibits α-glucosidase and α-amylase, enzymes involved in carbohydrate digestion, thereby slowing glucose absorption.
It also enhances insulin sensitivity in peripheral tissues and may stimulate insulin secretion from pancreatic β-cells. Additionally, the inulin content (a type of fructooligosaccharide) helps stabilize blood sugar levels by slowing glucose absorption. Dandelion root extract exhibits prebiotic activity primarily through its high inulin content, which selectively nourishes beneficial gut bacteria such as Bifidobacteria and Lactobacilli. This prebiotic effect contributes to improved gut microbiome composition, enhanced gut barrier function, and reduced intestinal inflammation.
The mild laxative effect of dandelion root is attributed to its bitter compounds stimulating digestive secretions and its inulin content, which adds bulk to stool and promotes regular bowel movements. Emerging research suggests potential anti-cancer properties through multiple mechanisms. Dandelion root extract induces apoptosis (programmed cell death) in various cancer cell lines, inhibits cell proliferation by affecting cell cycle regulation, and reduces angiogenesis (formation of new blood vessels) that tumors require for growth. It also shows anti-metastatic properties by inhibiting matrix metalloproteinases (MMPs) involved in cancer cell invasion.
The immunomodulatory effects of dandelion root are primarily mediated by its polysaccharides, which enhance natural killer (NK) cell activity, promote macrophage phagocytosis, and modulate cytokine production to balance immune responses. This may contribute to its traditional use for supporting immune function. Additionally, dandelion root extract has shown antimicrobial properties against various pathogens, including certain bacteria and fungi, though this activity is generally mild compared to conventional antimicrobials. The extract also demonstrates mild hypotensive effects through vasodilation, mediated by nitric oxide production and calcium channel modulation.
These diverse mechanisms of action explain dandelion root’s wide range of traditional and modern therapeutic applications, particularly for digestive, liver, and metabolic health.
Optimal Dosage
Disclaimer: The following dosage information is for educational purposes only. Always consult with a healthcare provider before starting any supplement regimen, especially if you have pre-existing health conditions, are pregnant or nursing, or are taking medications.
The typical dosage range for dandelion root extract supplements varies by preparation method and concentration. For dried root powder, 2-8 grams daily is common. For liquid extracts (1:5 tincture), 3-5 mL (approximately 60-100 drops) taken 2-3 times daily is standard. Standardized extracts typically range from 500-1500 mg daily, divided into 2-3 doses.
By Condition
Condition | Dosage | Notes |
---|---|---|
Liver support and detoxification | 500-1500 mg of standardized extract daily, or 4-6 grams of dried root powder daily, divided into 2-3 doses | Best taken between meals to maximize bile stimulation effects. May be used as part of a comprehensive detoxification program for 2-4 weeks, followed by a maintenance dose. |
Digestive support | 3-5 mL of liquid extract (1:5) before meals, or 1-2 grams of dried root powder 15-30 minutes before meals | The bitter compounds in dandelion root work best when tasted, so liquid extracts may be more effective for digestive stimulation when a small amount is held briefly in the mouth before swallowing. |
Mild edema and water retention | 4-10 grams of dried root as tea (decoction), or 2-4 mL of liquid extract 3 times daily | Effects typically begin within 1-2 hours and may last 4-6 hours. Increased fluid intake is recommended to support the diuretic effect. |
Blood sugar management | 1-2 grams of dried root powder 3 times daily with meals, or 500-1000 mg of standardized extract daily | Should be used as an adjunct to conventional treatment for diabetes, not as a replacement. Blood glucose monitoring is essential when using dandelion for this purpose. |
Prebiotic support for gut health | 4-10 grams of dried root powder daily, or 2-4 cups of roasted dandelion root tea daily | The inulin content provides prebiotic effects. Start with lower doses and gradually increase to avoid temporary digestive discomfort from increased fermentation in the gut. |
Mild constipation | 4-6 grams of dried root powder daily, or 2-3 cups of strong dandelion root tea daily | Effects are gentle and may take 1-3 days to become noticeable. Adequate hydration enhances effectiveness. |
By Age Group
Age Group | Dosage | Notes |
---|---|---|
Adults (18-65 years) | Standard dosages as listed above | Generally well-tolerated in this age group. Start with lower doses and increase gradually. |
Older adults (>65 years) | Start with 50-75% of standard adult dosage | Monitor for potential interactions with medications commonly used in this age group. May be particularly beneficial for age-related digestive changes and mild constipation. |
Children (12-17 years) | 50-75% of adult dosage, based on weight | Limited research in pediatric populations. Should only be used under healthcare provider supervision. |
Children under 12 years | Not recommended without professional guidance | Insufficient safety data for this age group. |
Pregnant or breastfeeding women | Not recommended | Insufficient safety data for use during pregnancy or lactation. May have mild hormonal effects that could affect pregnancy. |
By Form
Form | Dosage | Notes |
---|---|---|
Dried root powder | 2-8 grams daily, divided into 2-3 doses | Can be encapsulated, added to foods, or prepared as decoction (simmered in water for 10-15 minutes). |
Liquid extract (1:5 tincture) | 3-5 mL (60-100 drops), 2-3 times daily | Typically prepared with 45-60% alcohol. Can be diluted in water or juice. Faster absorption than solid forms. |
Standardized extract (2-5% sesquiterpene lactones) | 500-1500 mg daily, divided into 2-3 doses | Higher potency, more consistent active compound content. |
Tea/decoction | 1-2 teaspoons (2-4 grams) of dried root per cup of water, simmered for 10-15 minutes, 2-3 cups daily | Traditional form, may be less potent but provides hydration benefits. Bitter taste can be modified with honey or lemon. |
Roasted root (coffee substitute) | 1-2 teaspoons per cup, 2-3 cups daily | Roasting reduces bitter compounds but preserves some beneficial effects. Popular as a caffeine-free coffee alternative. |
Timing Considerations
For digestive support, take 15-30 minutes before meals to stimulate digestive secretions. For liver support, taking between meals may maximize bile stimulation. For diuretic effects, morning and early afternoon dosing is preferable to avoid nighttime urination. When used for prebiotic effects, consistent daily dosing is important to maintain beneficial changes in gut microbiota.
Bioavailability
Absorption Rate
The bioavailability of dandelion root extract varies significantly depending on the specific compounds and preparation methods. Water-soluble components like phenolic acids and inulin have moderate bioavailability (estimated at 10-30%),
while fat-soluble compounds like sesquiterpene lactones and triterpenes have lower bioavailability (5-15%) unless consumed with dietary fats. Liquid extracts generally demonstrate higher bioavailability than solid forms due to pre-solubilization of active compounds. The bitter compounds in dandelion root can stimulate digestive secretions
when
they contact taste receptors in the mouth, potentially enhancing the absorption of other compounds in the extract.
Enhancement Methods
Consuming dandelion root extract with a small amount of dietary fat enhances the absorption of fat-soluble components like sesquiterpene lactones and triterpenes, Liquid extracts (tinctures) generally have higher bioavailability than solid forms due to pre-solubilization of active compounds, Holding liquid extracts briefly in the mouth before swallowing activates bitter taste receptors, stimulating digestive secretions that may enhance absorption, Standardized extracts with higher sesquiterpene lactone content may offer improved bioavailability of these specific compounds, Combining with black pepper extract (piperine) may enhance absorption of certain compounds through inhibition of first-pass metabolism, Liposomal delivery systems can significantly improve bioavailability by protecting compounds from degradation and enhancing cellular uptake, Taking dandelion root extract on an empty stomach may increase absorption of some compounds, while taking with meals may enhance absorption of fat-soluble components
Timing Recommendations
For digestive benefits, dandelion root extract is most effective when taken 15-30 minutes before meals to allow bitter compounds to stimulate digestive secretions. For liver support, taking between meals may maximize bile stimulation effects. For diuretic effects, morning and early afternoon dosing is preferable to avoid nighttime urination. When used for prebiotic effects, consistent daily dosing is important to maintain beneficial changes in gut microbiota.
For blood sugar regulation, taking with meals may help moderate post-prandial glucose spikes.
Metabolism And Excretion
Metabolism: Phenolic compounds in dandelion root extract undergo extensive phase II metabolism in the liver, primarily through glucuronidation, sulfation, and methylation. Sesquiterpene lactones are metabolized through glutathione conjugation and other detoxification pathways. Some compounds are metabolized by intestinal microbiota before absorption, particularly complex polysaccharides like inulin, which are fermented to produce short-chain fatty acids.
Excretion: Metabolites are primarily excreted through urine, with a smaller portion eliminated via biliary excretion into feces. The diuretic effect of dandelion root may enhance urinary excretion of water-soluble metabolites. The elimination half-life of most active compounds ranges from 3-8 hours, though inulin and other prebiotic components have longer residence times in the digestive tract.
Factors Affecting Bioavailability
Age: Older adults may have reduced absorption due to decreased gastrointestinal function and altered liver metabolism, Gastrointestinal pH: Altered stomach acidity can affect the solubility and stability of certain compounds, particularly sesquiterpene lactones, Intestinal transit time: Faster transit reduces contact time for absorption, while slower transit may enhance absorption of some compounds, Gut microbiome composition: Influences metabolism of inulin and other compounds before absorption, affecting the production of beneficial metabolites, Concurrent medications: May compete for absorption or metabolic pathways, particularly medications processed by the liver, Food interactions: High-fiber meals may reduce absorption of some compounds, while fatty meals may enhance absorption of fat-soluble components, Processing methods: Heat treatment during manufacturing can alter compound stability and bioavailability, particularly for heat-sensitive sesquiterpene lactones, Extraction solvents: Water, alcohol, or mixed solvents extract different profiles of compounds with varying bioavailability
Bioactive Compounds Bioavailability
Compound | Bioavailability | Notes |
---|---|---|
Sesquiterpene lactones (taraxacin, taraxinic acid) | 5-15%, improved when consumed with fats | Bitter compounds that may stimulate digestive secretions when tasted, potentially enhancing overall absorption |
Phenolic acids (chicoric acid, chlorogenic acid, caffeic acid) | 10-30% | Undergo extensive first-pass metabolism; metabolites may retain biological activity |
Triterpenes (taraxasterol, taraxerol) | 5-15%, improved when consumed with fats | Fat-soluble compounds with limited water solubility |
Inulin and other fructooligosaccharides | Limited systemic absorption | Primarily act locally in the gastrointestinal tract as prebiotics; fermented by gut bacteria to produce beneficial short-chain fatty acids |
Minerals (potassium, iron, calcium) | Variable (10-40%) | Absorption affected by phytate and oxalate content; potassium has relatively high bioavailability |
Safety Profile
Safety Rating
Side Effects
- Mild gastrointestinal discomfort (occasional)
- Increased urination (expected pharmacological action, not adverse)
- Allergic reactions (rare, more common in individuals with existing allergies to plants in the Asteraceae family)
- Heartburn or acid reflux (occasional, due to bitter compounds stimulating digestive secretions)
- Mild hypoglycemia (rare, primarily in individuals taking anti-diabetic medications)
- Temporary increase in bowel movements (due to mild laxative effect)
- Contact dermatitis (rare, primarily with fresh plant contact rather than processed extracts)
Contraindications
- Known hypersensitivity to dandelion or plants in the Asteraceae family (including ragweed, chrysanthemums, marigolds, daisies)
- Bile duct obstruction or gallstones (due to choleretic effects that increase bile flow)
- Gastric hyperacidity or peptic ulcer disease (may exacerbate symptoms due to stimulation of gastric acid)
- Pregnancy and lactation (due to insufficient safety data and potential hormonal effects)
- Severe kidney disease (due to potassium content and diuretic effects)
- Children under 12 years (due to insufficient safety data)
Drug Interactions
Category | Interaction | Management |
---|---|---|
Diuretics | May enhance diuretic effects and potentially affect electrolyte balance | Monitor hydration status and electrolytes; may need to adjust diuretic dosage |
Anti-diabetic medications | May enhance hypoglycemic effects, potentially leading to low blood sugar | Monitor blood glucose levels closely; dose adjustment of medications may be necessary |
Anticoagulant/antiplatelet medications | Theoretical interaction due to vitamin K content, though clinically significant effects are rare | Monitor coagulation parameters if used concurrently with warfarin |
Medications metabolized by cytochrome P450 enzymes | May affect metabolism of certain drugs, though evidence is limited | Use with caution when taking medications with narrow therapeutic windows |
Lithium | Diuretic effect of dandelion may affect lithium excretion, potentially altering blood levels | Monitor lithium levels if used concurrently |
Medications that increase photosensitivity | Theoretical concern for additive photosensitizing effects, though evidence is limited | Use caution with sun exposure when combining with photosensitizing drugs |
Medications affected by changes in gastric pH | Bitter compounds may increase gastric acid secretion, potentially affecting drug absorption | Separate administration times if concerned about interaction |
Potassium-sparing diuretics | Potential for additive effects on potassium retention due to dandelion’s potassium content | Monitor potassium levels if used concurrently |
Upper Limit
No established upper limit. Clinical studies have used doses up to 8 grams of dried root daily without significant adverse effects. Traditional use suggests safety at typical recommended doses, but long-term safety data for high doses is limited.
Special Precautions
Medical Conditions: Individuals with gallbladder disease, gastroesophageal reflux disease (GERD), kidney disorders, or diabetes should use with caution and under medical supervision.
Surgery: Discontinue at least 2 weeks before scheduled surgery due to potential effects on blood glucose, blood pressure, and mild anticoagulant effects.
Allergies: Individuals with allergies to plants in the Asteraceae family (ragweed, chrysanthemums, marigolds, daisies) may have cross-reactivity to dandelion.
Monitoring: Those using dandelion for blood sugar or diuretic effects should regularly monitor relevant parameters.
Toxicity
Acute: Very low acute toxicity. Animal studies show LD50 values far exceeding therapeutic doses.
Chronic: Limited long-term toxicity studies, but traditional long-term use suggests safety at recommended doses.
Genotoxicity: No evidence of genotoxicity in available studies.
Carcinogenicity: No evidence of carcinogenic potential; some studies suggest potential anti-cancer properties.
Safety In Special Populations
Pediatric: Limited data available for children under 12 years; use with caution and only under healthcare provider supervision. Generally considered safe for children over 12 at adjusted doses.
Geriatric: Generally well-tolerated; monitor for potential interactions with medications commonly used in this population. May need dose adjustment due to potential changes in kidney or liver function.
Renal Impairment: Use with caution due to potassium content and diuretic effects. Not recommended in severe renal impairment.
Hepatic Impairment: Generally considered beneficial for mild hepatic impairment, but limited data for severe liver disease.
Pregnancy: Traditionally used as a galactagogue (to increase breast milk production) postpartum, but insufficient safety data for use during pregnancy. May have hormonal effects that could affect pregnancy. Generally not recommended.
Lactation: Traditionally used to enhance milk production, but scientific evidence is limited. Use with caution.
Allergenic Potential
Low to moderate. Individuals with allergies to plants in the Asteraceae family (ragweed, chrysanthemums, marigolds, daisies) may have cross-reactivity to dandelion. Allergic reactions are rare but may include skin rash, itching, or in severe cases, anaphylaxis.
Regulatory Status
Fda Status
In the United States, dandelion root extract is regulated as a dietary supplement under the Dietary Supplement Health and Education Act (DSHEA) of 1994. This classification means it is not subject to pre-market approval for safety and efficacy, but manufacturers are responsible for ensuring their products are safe before marketing and that any claims made are not false or misleading. The FDA has not approved any specific health claims for dandelion root extract. Manufacturers can make structure/function claims (e.g., ‘supports liver health’ or ‘promotes healthy digestion’) but cannot make disease claims (e.g., ‘treats hepatitis’ or ‘cures gallstones’) without going through the drug approval process.
Dandelion is generally recognized as safe (GRAS) for use in foods when used in normal culinary amounts. Dandelion root is included in the FDA’s list of ‘Herbs of Undefined Safety’ due to insufficient toxicological data rather than known safety concerns.
International Status
Eu: In the European Union, dandelion root has been evaluated by the European Medicines Agency (EMA) Committee on Herbal Medicinal Products (HMPC). The EMA has established a Community herbal monograph for dandelion root, recognizing its traditional use for mild digestive disorders, temporary loss of appetite, and to increase the amount of urine to achieve flushing of the urinary tract. Products containing dandelion root can be registered as Traditional Herbal Medicinal Products (THMPs) if they meet quality standards and have been in medicinal use for at least 30 years (including at least 15 years within the EU). Dandelion is also approved for use in food supplements under the Food Supplements Directive 2002/46/EC.
Canada: Health Canada has included dandelion root in the Natural Health Products Ingredients Database with a medicinal ingredient monograph. It is approved for use in Natural Health Products (NHPs) with several permitted claims, including as a hepatoprotectant, choleretic, digestive aid, and diuretic. Products must meet the quality requirements outlined in the Natural Health Products Regulations and obtain a Natural Product Number (NPN) before being marketed.
Australia: The Australian Therapeutic Goods Administration (TGA) lists dandelion root as an approved ingredient for listed complementary medicines. It is included in the Therapeutic Goods (Permissible Ingredients) Determination with specific requirements and restrictions. Products containing dandelion must be listed on the Australian Register of Therapeutic Goods (ARTG) before they can be marketed.
Uk: Post-Brexit, the UK continues to recognize dandelion products registered as THMPs under the previous EU system. The Medicines and Healthcare products Regulatory Agency (MHRA) maintains similar standards to the EMA for herbal products.
Germany: In Germany, dandelion root has been evaluated by Commission E (the German regulatory authority for herbs) and is approved for use in disturbances in bile flow, stimulation of diuresis, loss of appetite, and dyspeptic complaints. It has a positive monograph, indicating official recognition of its medicinal uses.
Labeling Requirements
Us: In the US, dandelion root supplements must be labeled as dietary supplements and include a Supplement Facts panel listing the amount of dandelion root or extract per serving. They must include the standard FDA disclaimer: ‘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.’ Any structure/function claims must be accompanied by this disclaimer.
Eu: In the EU, products registered as THMPs must include specific approved indications based on traditional use, recommended dosage, and appropriate warnings. Food supplements must comply with the Food Supplements Directive labeling requirements, including recommended daily dose and warning statements.
Warnings: Common required warnings across jurisdictions include: not for use during pregnancy and lactation without medical advice; keep out of reach of children; consult healthcare practitioner before use if taking medications or have medical conditions, particularly gallbladder disease, bile duct obstruction, or kidney disorders; discontinue use if hypersensitivity reactions occur.
Regulatory Challenges
Standardization: One of the primary regulatory challenges for dandelion root products is the lack of universally accepted standardization parameters. Different manufacturers may standardize to different compounds (e.g., sesquiterpene lactones, inulin, or total phenolics) or may not standardize at all, leading to product variability.
Claim Limitations: The restriction on disease claims limits manufacturers’ ability to communicate some of the better-researched benefits of dandelion, particularly for liver and gallbladder health, where traditional use is well-established but cannot be explicitly stated on product labels in many jurisdictions.
Quality Control: Ensuring consistent quality and accurate species identification remains a challenge. Adulteration with similar-looking roots or confusion between different Taraxacum species can occur.
Sustainable Sourcing: As demand increases, ensuring sustainable wild-harvesting practices or transitioning to cultivated sources presents regulatory and supply chain challenges.
Recent Regulatory Developments
In recent years,
there has been increased regulatory scrutiny of herbal products globally, with more emphasis on quality control, standardization, and evidence-based approaches. The European Food Safety Authority (EFSA) has been evaluating health claims for botanicals, though most evaluations have been on hold pending resolution of the broader regulatory framework for botanicals in the EU.
There is growing interest from regulatory bodies in the potential health benefits of dandelion root, particularly its hepatoprotective and prebiotic properties, though
this has not yet translated into approved health claims in most regions. Some countries are developing more specific quality standards for dandelion products, including testing requirements for potential contaminants like heavy metals and pesticides.
Food Vs Supplement Classification
Dandelion root has a dual status in many jurisdictions as both a food and a supplement ingredient. Roasted dandelion root is widely used as a coffee substitute and is generally regulated as a conventional food. More concentrated extracts or formulations making health claims are typically regulated as supplements or herbal medicines.
This dual classification can create regulatory complexities, particularly for products that fall in the gray area between food and supplement, such as dandelion root teas that make health claims.
Synergistic Compounds
Compound | Synergy Mechanism | Evidence Rating |
---|---|---|
Milk Thistle (Silybum marianum) | Both herbs support liver health through complementary mechanisms. While milk thistle primarily protects hepatocytes and promotes regeneration through silymarin, dandelion root enhances bile flow and liver detoxification pathways. This combination provides comprehensive liver support, particularly beneficial for conditions involving both hepatocyte damage and cholestasis. | 3 |
Artichoke Leaf Extract (Cynara scolymus) | Both herbs have choleretic effects (stimulating bile production) but through different active compounds. Artichoke’s cynarin and chlorogenic acid complement dandelion’s sesquiterpene lactones, providing enhanced bile stimulation and digestive support. Both also have antioxidant properties that may protect the liver from oxidative damage. | 2 |
Burdock Root (Arctium lappa) | Both roots contain inulin and bitter compounds that support digestive health and liver function. Burdock adds blood-purifying properties and skin health benefits to dandelion’s detoxification support. This traditional combination is used in many herbal detoxification formulas. | 2 |
Yellow Dock Root (Rumex crispus) | Yellow dock complements dandelion’s liver support with additional mild laxative effects and iron content. Together they support both liver detoxification and elimination pathways, helping to prevent the reabsorption of toxins. This combination is traditionally used for skin conditions related to poor elimination. | 2 |
Turmeric (Curcuma longa) | Both have anti-inflammatory and antioxidant properties through different pathways. Turmeric’s curcuminoids primarily inhibit NF-κB and COX-2, while dandelion has broader effects on inflammatory mediators. Turmeric also enhances bile production, complementing dandelion’s choleretic effects. This combination provides comprehensive support for inflammatory conditions, particularly those affecting the digestive system. | 2 |
Ginger (Zingiber officinale) | Ginger’s warming, circulatory-enhancing properties complement dandelion’s cooling, detoxifying effects. Ginger also adds carminative (gas-relieving) properties that enhance dandelion’s digestive benefits. Both have anti-inflammatory effects through different pathways, providing more comprehensive inflammation modulation. | 2 |
Probiotics (Lactobacillus and Bifidobacterium species) | Dandelion root’s inulin content provides prebiotic fiber that nourishes beneficial gut bacteria, while probiotics directly supplement these beneficial strains. This synergistic relationship supports a healthy gut microbiome, enhanced digestion, and improved immune function. | 2 |
Licorice Root (Glycyrrhiza glabra) | Licorice’s demulcent (soothing) properties balance dandelion’s bitter stimulating effects, making the combination gentler on the digestive system. Both herbs support liver health through different mechanisms. Note: Only use small amounts of licorice or deglycyrrhizinated licorice (DGL) for long-term use to avoid potential side effects. | 2 |
Peppermint (Mentha piperita) | Peppermint’s carminative and antispasmodic properties complement dandelion’s bitter digestive stimulant effects. Peppermint also improves the palatability of dandelion preparations. This combination is particularly beneficial for digestive discomfort with bloating or spasm. | 2 |
Berberine-containing herbs (Goldenseal, Oregon Grape, Barberry) | Berberine’s antimicrobial and blood glucose-regulating properties complement dandelion’s liver support and mild hypoglycemic effects. This combination may be particularly beneficial for digestive infections or dysbiosis and metabolic conditions. | 1 |
Chicory Root (Cichorium intybus) | Both are closely related plants in the Asteraceae family with similar constituents, including inulin and bitter compounds. Chicory adds additional prebiotic effects and slightly different bitter principles, enhancing overall digestive and liver support. | 2 |
Black Pepper Extract (Piperine) | Piperine can enhance the bioavailability of various compounds in dandelion root by inhibiting certain detoxification enzymes that would otherwise metabolize these compounds before they can be absorbed. This may increase the potency and effectiveness of dandelion root extract. | 1 |
Vitamin C | Vitamin C enhances dandelion’s antioxidant effects and may improve iron absorption from dandelion, which contains naturally occurring iron. Both support immune function and detoxification processes. | 1 |
Zinc | Zinc supports many of the enzyme systems involved in detoxification that dandelion helps to promote. It also supports immune function and skin health, complementing dandelion’s traditional uses for these systems. | 1 |
Antagonistic Compounds
Compound | Interaction Type | Evidence Rating |
---|---|---|
Diuretic medications | Dandelion’s diuretic properties may enhance the effects of pharmaceutical diuretics, potentially leading to increased fluid loss and electrolyte imbalances. This is particularly concerning with loop diuretics like furosemide (Lasix). | 2 |
Anti-diabetic medications | Dandelion may enhance the blood glucose-lowering effects of anti-diabetic drugs, potentially leading to hypoglycemia. This includes insulin, sulfonylureas, meglitinides, and other medications that lower blood sugar. | 2 |
Anticoagulant/antiplatelet medications | Dandelion contains vitamin K, which could theoretically reduce the effectiveness of vitamin K antagonists like warfarin. However, the vitamin K content in typical supplement doses is relatively low, making clinically significant interactions uncommon. | 1 |
Medications metabolized by cytochrome P450 enzymes | Some compounds in dandelion may inhibit certain cytochrome P450 enzymes, potentially affecting the metabolism of drugs processed by these pathways. This could increase blood levels and effects of these medications. | 1 |
Lithium | Dandelion’s diuretic properties may affect lithium excretion, potentially altering blood levels. This could increase the risk of lithium toxicity or reduced efficacy. | 1 |
Proton pump inhibitors and antacids | These medications reduce stomach acid, which may counteract dandelion’s bitter stimulating effects on digestive secretions. Conversely, dandelion may partially counteract the acid-reducing effects of these medications. | 1 |
Potassium-sparing diuretics | Dandelion is naturally high in potassium. When combined with potassium-sparing diuretics like spironolactone, there is a theoretical risk of hyperkalemia (elevated potassium levels). | 1 |
Ciprofloxacin and other quinolone antibiotics | Dandelion contains minerals that may bind to these antibiotics in the digestive tract, potentially reducing their absorption and effectiveness. | 1 |
Medications that increase photosensitivity | Theoretical concern for additive photosensitizing effects, though evidence is limited. Medications that may increase sun sensitivity include certain antibiotics, retinoids, and some psychiatric medications. | 1 |
Tannin-containing herbs (black tea, oak bark, witch hazel) | Tannins may bind to and reduce absorption of dandelion’s active compounds. Separating administration times is advisable. | 1 |
Alcohol | May enhance the diuretic effects of dandelion, potentially leading to increased dehydration. Alcohol may also increase the burden on the liver, potentially counteracting some of dandelion’s hepatoprotective benefits. | 1 |
Stimulant laxatives (senna, cascara) | Dandelion has mild laxative properties. When combined with stronger stimulant laxatives, there is potential for additive effects leading to excessive bowel stimulation and possible electrolyte imbalances. | 1 |
Cost Efficiency
Relative Cost
Low
Cost Per Effective Dose
The typical cost for dandelion root extract supplements ranges from $0.10 to $0.40 per 500-1000 mg dose, depending on brand, formulation, and quality. For a standard daily dose, this translates to approximately $3-12 per month for supplementation.
Value Analysis
Dandelion root extract offers excellent value for its cost when compared to other supplements with similar applications. For liver support, it provides a cost-effective alternative to more expensive options like milk thistle or artichoke extract, with complementary mechanisms of action. For digestive health, it is significantly less expensive than many digestive enzymes or specialized gut health formulations. As a gentle detoxifying agent, it offers a natural, affordable alternative to many commercial detox formulations.
The relatively low cost is due to dandelion’s abundance, ease of cultivation, and minimal processing requirements for basic preparations.
Price Comparison
Supplement Forms
- Basic dried root powder (500-1000 mg capsules) typically ranges from $5-15 for a 30-60 day supply, making it the most cost-effective form.
- Standardized extracts range from $10-25 for a 30-day supply, offering more consistent potency at a moderate price increase.
- Tinctures and liquid extracts range from $10-30 for a 1-2 oz bottle (approximately 30-day supply), offering potentially better absorption but at a higher cost.
- Roasted dandelion root coffee substitute ranges from $8-20 per package (approximately 20-40 servings), offering both culinary enjoyment and mild health benefits.
Competing Products
- Compared to milk thistle ($10-30/month), artichoke extract ($15-35/month), or specialized liver support formulas ($20-50/month), dandelion root ($3-12/month) offers competitive or superior value.
- Compared to digestive enzymes ($15-40/month), specialized probiotics ($20-50/month), or digestive bitters ($12-30/month), dandelion provides good complementary benefits at a lower average cost.
- Compared to commercial detox formulations ($20-60/month), dandelion offers a simple, natural alternative at a fraction of the cost.
- Compared to specialized prebiotic supplements ($15-40/month), dandelion root provides natural inulin content at a lower cost, though with less precise dosing of prebiotic fiber.
Factors Affecting Cost
Harvesting method (wild-harvested vs. cultivated), Organic certification (organic products typically cost 20-50% more), Processing method (simple drying vs. extraction processes), Standardization (standardized extracts cost more but offer more consistent potency), Brand positioning and marketing approach, Packaging (sustainable or premium packaging increases costs), Third-party testing and certifications, Geographic source (European sources often command premium prices)
Cost Saving Strategies
Bulk Purchasing: Buying larger quantities can reduce the per-dose cost by 20-40%.
Subscription Services: Many supplement companies offer subscription discounts of 10-15% for regular deliveries.
Combination Products: For certain applications, combination products containing dandelion along with synergistic compounds may offer better value than purchasing supplements separately.
Growing Your Own: Dandelion is easily grown or wild-harvested in many regions, offering significant cost savings for those willing to process it themselves.
Tea Form: Preparing dandelion root tea from dried root is generally less expensive per dose than capsules or extracts, though it may contain lower concentrations of certain compounds.
Cost Effectiveness By Application
Liver Support
- High
- Good preclinical evidence supports efficacy, and cost is lower than many alternatives with similar hepatoprotective effects.
Digestive Health
- High
- Traditional use and mechanism of action support benefits for digestive function at a very reasonable cost.
Gentle Detoxification
- Medium to High
- Provides natural support for elimination pathways at a fraction of the cost of commercial detox formulations, though with less marketing hype.
Prebiotic Support
- Medium
- Natural source of inulin at a reasonable cost, though specialized prebiotic supplements provide more precise dosing of specific fibers.
Diuretic Effect
- High
- Gentle, potassium-sparing diuretic effect at a very low cost compared to pharmaceutical alternatives, though with milder action.
Blood Sugar Regulation
- Low to Medium
- Emerging evidence supports benefits, but should be used as a complement to, not replacement for, conventional management.
Stability Information
Shelf Life
Properly stored dried dandelion root typically has a shelf life of 1-2 years. Encapsulated or tableted extracts generally have a shelf life of 2-3 years. Liquid extracts (tinctures) typically have a shelf life of 3-5 years due to the preservative effect of alcohol. Roasted dandelion root (coffee substitute) has a shelf life of 1-2 years when properly stored.
Storage Recommendations
Store in a cool, dry place away from direct sunlight. Optimal temperature range is 15-25°C (59-77°F). Avoid exposure to high humidity. Keep container tightly closed when not in use. Dried root and solid extract forms should be stored in airtight containers, preferably opaque or amber to protect from light. Liquid extracts should be stored in tightly sealed amber glass bottles. Refrigeration is not necessary but may extend shelf life, particularly for alcohol-free liquid preparations.
Degradation Factors
Light exposure: UV radiation can degrade sesquiterpene lactones and other active compounds, Heat: Temperatures above 40°C (104°F) can accelerate degradation of thermolabile compounds, particularly sesquiterpene lactones, Oxygen: Exposure to air promotes oxidation of phenolic compounds and other antioxidants, Moisture: High humidity can promote hydrolysis reactions and microbial growth, Microbial contamination: Improper drying or storage can lead to mold or bacterial growth, Enzymatic activity: Residual plant enzymes can degrade active compounds if not properly deactivated during processing
Stability In Different Formulations
Dried Root: Relatively stable when properly dried and stored, though gradual loss of volatile compounds and oxidation of phenolics occurs over time. Typical shelf life: 1-2 years.
Capsules Tablets: More stable than raw herb due to reduced surface area exposure to air. Excipients may provide additional stability. Typical shelf life: 2-3 years.
Liquid Extracts: Alcohol-based extracts (tinctures) are highly stable due to the preservative effect of alcohol. Glycerites and alcohol-free extracts are less stable and may require refrigeration after opening. Typical shelf life: 3-5 years for alcohol-based, 1-2 years for alcohol-free.
Roasted Root: The roasting process reduces some active compounds but creates more stable end product for use as coffee substitute. Typical shelf life: 1-2 years.
Standardized Extracts: Stability varies based on the specific compounds standardized and the extraction process. Generally stable when properly formulated with appropriate excipients. Typical shelf life: 2-3 years.
Stability Testing Methods
High-performance liquid chromatography (HPLC) to monitor levels of key compounds like sesquiterpene lactones and phenolic acids over time, Thin-layer chromatography (TLC) for qualitative assessment of compound degradation, Spectrophotometric analysis to track changes in total phenolic content, Inulin content analysis to monitor polysaccharide stability, Accelerated stability testing at elevated temperatures and humidity, Microbial testing to ensure absence of pathogenic growth during storage, Organoleptic evaluation (color, odor, taste) for quality control
Stabilization Techniques
Antioxidants: Addition of natural antioxidants like vitamin E or rosemary extract can help prevent oxidation of phenolic compounds and sesquiterpene lactones.
Desiccants: Silica gel packets included in packaging can reduce moisture exposure, particularly important for powdered forms.
Nitrogen Flushing: Replacing oxygen with nitrogen in the package headspace can significantly reduce oxidative degradation.
Vacuum Packaging: Removing air from packaging reduces oxidation potential.
Proper Drying: Initial proper drying to optimal moisture content (typically <10%) is critical for long-term stability.
Standardization: Standardizing extracts to specific marker compounds can help ensure consistent potency despite some natural degradation over time.
Stability After Opening
Dried root and solid dosage forms remain relatively stable for 6-12 months after opening if properly resealed and stored according to recommendations. Liquid extracts maintain stability for 1-2 years after opening if properly sealed between uses. Roasted dandelion root coffee substitute should ideally be used within 3-6 months after opening to maintain optimal flavor and aroma.
Special Considerations
Sesquiterpene lactones, key active compounds in dandelion root, are relatively unstable and sensitive to heat, light, and oxidation. Products standardized to these compounds may show more significant potency loss over time compared to those standardized to more stable compounds. The bitter taste of dandelion root preparations may diminish over time, which can be an indicator of degradation of sesquiterpene lactones and other bitter principles. This taste change may occur before significant changes in overall medicinal activity.
Inulin, a major component of dandelion root, is relatively stable under proper storage conditions but can degrade with exposure to high heat or acidic conditions. Products with high inulin content should be protected from these factors to maintain prebiotic activity.
Sourcing
Natural Sources
- Taraxacum officinale (Common Dandelion) – primary commercial source, native to Europe but naturalized worldwide
- Taraxacum erythrospermum (Red-seeded Dandelion) – less commonly used, but contains similar compounds
- Taraxacum japonicum (Japanese Dandelion) – used in East Asian traditional medicine
- Taraxacum coreanum (Korean Dandelion) – used in Korean traditional medicine
- Taraxacum mongolicum (Chinese Dandelion) – used in Traditional Chinese Medicine (TCM)
Cultivation And Harvesting
- Dandelion thrives in a wide range of conditions but prefers well-drained, fertile soil with full sun to partial shade. It is highly adaptable and can grow in various climates, from temperate to subtropical regions. For commercial cultivation, consistent moisture and moderate temperatures produce the highest quality roots with optimal active compound content.
- Dandelion is considered a sustainable crop as it requires minimal inputs, has few pests, and can grow on marginal lands. It also improves soil health through its deep taproot, which breaks up compacted soil and brings nutrients to the surface. Wild harvesting should be done selectively, avoiding areas with potential contamination from pesticides, heavy metals, or pollutants.
- For medicinal use, roots are typically harvested in fall (autumn) of the first or second year when inulin content is highest and bitter compounds are most concentrated. Spring harvest is possible but yields roots with different phytochemical profiles. Harvesting involves carefully digging to extract the entire taproot, which can extend 12-18 inches into the soil. Mechanical harvesters are used for commercial production.
- Roots should be washed thoroughly to remove soil, then sliced lengthwise to facilitate drying. Proper drying at temperatures below 40°C (104°F) is critical to preserve active compounds. Roots are considered properly dried when they snap cleanly rather than bend. Dried roots should be stored in airtight containers protected from light, heat, and moisture.
Extraction Methods
Method | Description | Compounds Extracted | Efficiency |
---|---|---|---|
Water extraction (decoction) | Roots are simmered in water for 10-15 minutes to extract water-soluble compounds including inulin, some phenolic acids, and minerals. Traditional method used for tea preparations. | Inulin, water-soluble phenolic compounds, minerals, some bitter compounds | Medium for water-soluble compounds, low for lipophilic compounds |
Hydroalcoholic extraction (tincture) | Uses a mixture of water and alcohol (typically 30-60% ethanol) to extract a broader spectrum of compounds. Common method for commercial extracts. | Sesquiterpene lactones, triterpenes, phenolic compounds, some inulin | High for most bioactive compounds |
Glycerin extraction (glycerite) | Uses glycerin as a solvent, producing an alcohol-free extract. Less efficient than alcohol but preferred for certain applications. | Similar profile to hydroalcoholic but in lower concentrations | Medium |
Supercritical CO2 extraction | Uses carbon dioxide under pressure to extract primarily lipophilic compounds. Produces a concentrated extract without solvent residues. | Sesquiterpene lactones, triterpenes, some phenolic compounds | High for lipophilic compounds, low for hydrophilic compounds |
Roasting | Roots are roasted at controlled temperatures to create a coffee substitute. This process reduces bitter compounds and creates new flavor compounds through Maillard reactions. | Modified profile with reduced bitter compounds and some degradation of heat-sensitive compounds | Low for medicinal compounds, but creates desirable flavor profile for beverage use |
Quality Considerations
High-quality dandelion root extract should meet several criteria: 1) Harvested at optimal time (fall of first or second year); 2) Properly dried to preserve active compounds; 3) Standardized content of key compounds (typically sesquiterpene lactones or inulin); 4) Free from contamination by heavy metals, pesticides, and microbes; 5) Properly identified species (Taraxacum officinale); 6) Sustainable harvesting or cultivation practices; 7) Appropriate extraction method for intended use; 8) Minimal processing to preserve natural compound profile; 9) Proper storage to prevent degradation; 10) Third-party testing for purity and potency.
Commercial Production
- Eastern Europe (particularly Poland, Bulgaria, and Hungary)
- China
- North America (particularly Pacific Northwest and Northeast regions)
- Germany
- France
- Standardization of active compounds due to natural variation based on growing conditions, harvest time, and post-harvest handling
- Efficient root harvesting, as the deep taproot can be difficult to extract completely
- Distinguishing from similar-looking plants during wild harvesting
- Ensuring consistent drying conditions to preserve active compounds
- Managing potential contamination from environmental pollutants when wild-harvested
Dandelion is generally considered a sustainable crop with minimal environmental impact. It requires few agricultural inputs, has natural pest resistance, and can grow on marginal lands. Wild harvesting should follow sustainable practices to prevent overharvesting, though dandelion’s abundance and rapid reproduction make this less of a concern than for many other medicinal plants. The plant’s deep root system helps prevent soil erosion and can help remediate some types of contaminated soil. Processing methods vary in their environmental impact, with water and alcohol extractions generally having lower environmental footprints than methods requiring more energy or synthetic solvents.
Regional Variations
- Dandelion’s phytochemical profile varies based on growing conditions, soil composition, climate, and harvest time. Plants grown in mineral-rich soils typically have higher mineral content. Colder climates may increase bitter compound production as a stress response. Regional subspecies may also have slightly different compound profiles. Fall-harvested roots generally have higher inulin content, while spring-harvested roots typically have higher bitter compound content.
- European producers often follow European Pharmacopoeia standards or the guidelines of the European Medicines Agency (EMA). North American producers may follow USP (United States Pharmacopeia) guidelines or AHPA (American Herbal Products Association) standards. Asian producers, particularly from China, may follow Chinese Pharmacopoeia standards, though many now produce to meet European or North American import requirements.
Historical Usage
Dandelion (Taraxacum officinale) has been used medicinally for thousands of years across multiple civilizations, with the root specifically valued for its distinct therapeutic properties. The plant’s name derives from the French ‘dent de lion’ (lion’s tooth), referring to its serrated leaves, while its genus name Taraxacum comes from the Persian ‘tarakhshaqun’ or Arabic ‘tarashaquq,’ indicating its ancient use in Middle Eastern medicine.
The earliest documented medicinal use of dandelion dates back to ancient China and the Arab world. Chinese physicians used dandelion as early as the 7th century CE, primarily for digestive disorders, inflammation, and as a liver tonic. The root was particularly valued for what Traditional Chinese Medicine (TCM) practitioners called ‘clearing heat and toxicity’ from the liver and gallbladder. In TCM, dandelion root was classified as bitter and cold, making it suitable for treating ‘hot’ conditions like infections, inflammations, and liver congestion.
In ancient Arabia and Persia, physicians including the renowned Avicenna (980-1037 CE) documented dandelion’s use as a liver remedy and diuretic in texts like ‘The Canon of Medicine.’ These early Arabic medical traditions influenced European medicine through the translation of medical texts during the Middle Ages.
Native American tribes independently discovered dandelion’s medicinal properties after it was introduced to North America by European settlers. The Iroquois, Ojibwe, and Mohegan tribes used dandelion root for kidney disease, digestive issues, and as a tonic. The Mohegan specifically prepared dandelion root as a blood purifier and liver tonic.
In European folk medicine, dandelion root gained prominence during the Middle Ages. The 10th-century Arab physicians in Spain introduced it to European medicine, and by the 13th century, it was commonly mentioned in Welsh medicines. The root was primarily used for liver complaints, digestive disorders, and as a blood purifier. Its diuretic properties gave rise to folk names like ‘pissenlit’ in French (literally ‘wet the bed’) and similar names in other European languages.
During the Renaissance period, European herbalists expanded dandelion root’s applications. The Swiss physician Paracelsus (1493-1541) prescribed it for various ailments including liver and spleen diseases. The influential 17th-century English herbalist Nicholas Culpeper wrote that dandelion ‘worketh mightily upon obstructions of the liver, gall and spleen,’ reflecting the traditional understanding of its hepatic benefits.
By the 18th and 19th centuries, dandelion root had become an established remedy in Western herbal medicine. It was listed in official pharmacopeias throughout Europe and North America. The Eclectic physicians of 19th-century America, who combined conventional and herbal medicine, frequently prescribed dandelion root for liver and gallbladder disorders, dyspepsia, and as a gentle laxative. The Eclectic medical text ‘King’s American Dispensatory’ (1898) provided detailed information on dandelion’s preparation and uses, noting its value as a hepatic stimulant and diuretic.
During this period, dandelion root also gained popularity as a coffee substitute, particularly during times of coffee shortages such as the American Civil War and both World Wars. The roasted root provided a caffeine-free alternative with a somewhat similar flavor profile and additional health benefits. This use continues today, with dandelion root coffee remaining popular in natural food markets.
In the early 20th century, with the rise of pharmaceutical medicine, dandelion root’s medicinal use declined in conventional practice but remained important in traditional herbalism. The renowned 20th-century herbalist Maria Treben of Austria championed dandelion root in her influential book ‘Health Through God’s Pharmacy’ (1980), particularly for liver and gallbladder complaints.
The latter part of the 20th century saw renewed scientific interest in dandelion root’s medicinal properties. Research began to validate many of its traditional uses, particularly its choleretic (bile-stimulating), hepatoprotective, and anti-inflammatory effects. Studies identified key active compounds including sesquiterpene lactones, triterpenes, phenolic compounds, and inulin, providing a scientific basis for its traditional applications.
In contemporary herbal medicine, dandelion root is valued for liver support, digestive health, and as a gentle detoxifying agent. It has become a common ingredient in herbal detoxification formulas, liver support supplements, and digestive bitters. The root is also increasingly recognized for its prebiotic properties due to its high inulin content, supporting its traditional use for digestive health from a modern perspective.
Beyond medicine, dandelion root has a rich culinary history. In addition to its use as a coffee substitute, the root has been used as a food source in various cultures. Young roots can be eaten as vegetables, similar to parsnips, and have been particularly important during times of food scarcity. In Korean cuisine, dandelion root is used in salads and side dishes, while in some European traditions, it is added to soups and stews.
Today, dandelion root continues to bridge traditional uses and modern applications. It is being investigated for potential benefits in conditions like non-alcoholic fatty liver disease, diabetes, and even cancer, while maintaining its traditional role in supporting digestive and liver health. This long history of use across diverse cultures speaks to dandelion root’s remarkable versatility and therapeutic potential, making it one of the most enduring medicinal plants in human history.
Scientific Evidence
Evidence Rating
Key Studies
Meta Analyses
Ongoing Trials
Investigation of dandelion root extract for chemoprevention in patients with high risk of colorectal cancer, Evaluation of standardized dandelion root extract for non-alcoholic fatty liver disease (NAFLD), Assessment of dandelion root extract’s effects on gut microbiome composition in healthy adults, Pilot study of dandelion root extract for mild digestive disorders
Research Gaps
Well-designed, larger-scale clinical trials in humans, Long-term safety and efficacy studies beyond 12 weeks, Standardization of extracts and identification of optimal active compound profiles, Comparative effectiveness studies against conventional treatments, Dose-response relationships for different indications, Pharmacokinetic studies of specific bioactive compounds, Effects on gut microbiome composition and function, Potential drug interactions, particularly with commonly used medications, Mechanisms of action in vivo, particularly for hepatoprotective and metabolic effects
Evidence By Application
Liver Support
- Moderate
- Good preclinical evidence from animal and in vitro studies, but limited clinical trials in humans. Traditional use is well-established.
Digestive Support
- Low to Moderate
- Primarily based on traditional use and pharmacological properties; limited clinical evidence but strong mechanistic plausibility.
Diuretic Effect
- Low to Moderate
- One small human study supports traditional use, though it used leaf rather than root extract. Mechanism is well-understood.
Blood Sugar Regulation
- Low
- Primarily based on animal studies and in vitro research; limited clinical evidence in humans.
Anti Inflammatory
- Low to Moderate
- Good preclinical evidence from in vitro and animal studies, but limited clinical trials in humans.
Prebiotic Effects
- Low
- Based on known inulin content and general research on inulin as a prebiotic; specific studies on dandelion root’s prebiotic effects are limited.
Anti Cancer
- Very Low
- Promising in vitro and animal studies, but very limited clinical evidence. Requires significantly more research before clinical applications.
Disclaimer: The information provided is for educational purposes only and is not intended as medical advice. Always consult with a healthcare professional before starting any supplement regimen, especially if you have pre-existing health conditions or are taking medications.