Equol (S-equol)
Also called S-equol, natural S-equol, SE5-OH, equol supplement.
Best grade B across 11 graded outcomes Other Last checked
The short answer
From 18 sourcesS-equol is the soy isoflavone metabolite that only some people's gut bacteria make. Supplements of about 10 mg a day reduced hot flushes in Japanese and US trials, and a 2019 meta-analysis of 5 trials found a benefit (grade B). The Menopause Society's 2023 statement still does not recommend equol for hot flashes, and most trials were small and industry-linked.
Every graded outcome on this page
11 rows · line = participants- BGrade BHot flushes in postmenopausal women (pooled)Hot flushesn 728
- BGrade BHot flush frequency in equol non-producersHot flushesn 160
- CGrade CMenopausal symptoms and moodMoodn 134
- CGrade CHot flash frequency vs soy isoflavones (active comparator)Hot flushesn 102
- CGrade CCrow's-feet wrinklesSkinn 101
- CGrade CMenopausal symptoms with soy isoflavones, by equol producer statusHot flushesn 96
- CGrade CBone resorption and whole-body bone densityBonen 93
- CGrade CBone turnover markers and whole-body bone density (with resveratrol)Bonen 60
- CGrade CClimacteric symptoms, skin AGEs and visceral fatHot flushesn 57
- CGrade CHbA1c, LDL cholesterol and arterial stiffness in overweight adultsMetabolicn 54
- DGrade DHand osteoarthritis pain and functionJoint painn 102
- 8 more graded outcomes, in the evidence chapter
Key facts
- What it is
- S-equol (C15H14O3) is made from daidzein by gut bacteria in about 50% of Asians and 25% of non-Asians, according to a 2015 review; supplements are made by fermenting soy germ with Lactococcus garvieae11310
- Hot flushes
- A 2019 meta-analysis of 5 randomized trials (728 women) found equol lowered hot flush scores; 3 trials were positive and 2 were not (B)4
- Largest single trial
- In 160 equol non-producing Japanese women, 10 mg a day for 12 weeks cut hot flush frequency by 58.7% vs 34.5% with placebo5
- Expert view
- The 2023 nonhormone therapy position statement of The North American Menopause Society lists the soy metabolite equol as not recommended for hot flashes (Level II, limited or inconsistent evidence)2
- Producers vs non-producers
- Most trials enrolled women who cannot make equol; in a 6-month soy isoflavone trial, symptoms improved only in women who could512
- How the body handles it
- Rapidly absorbed with a plasma half-life of about 8 hours; 82% of a 10 or 30 mg dose was recovered in urine10
- Safety data
- Trials of up to 1 year reported no serious adverse effects and no changes in sex or thyroid hormones; a 2015 review judged the limited safety data, including breast and endometrium, not a cause for concern7513
- Breast cancer hormone drugs
- 10 mg a day for 7 days did not significantly change blood levels of anastrozole, letrozole, exemestane or tamoxifen in 24 healthy postmenopausal women (6 per drug)17
What it is
S-equol is made by some people's gut bacteria from the soy isoflavone daidzein; supplements supply it ready-made from fermented soy germ.
How it works
ProposedS-equol is the form of equol that gut bacteria make from the soy isoflavone daidzein. It binds estrogen receptor beta selectively and, in vivo, antagonises dihydrotestosterone. Whether a person makes equol depends on their gut bacteria, which is the proposed reason soy isoflavones help some women's hot flushes and not others. Supplements made by fermenting soy germ with Lactococcus garvieae deliver S-equol directly, so they bypass producer status. How it reduces hot flushes is not established.10131214
Forms side by side: ready-made S-equol and soy isoflavones
2 forms named in our sources. The rest show what our data holds, and say plainly where it holds nothing yet.
Equol (S-equol) forms compared
2 forms| 2 forms | S-equol from fermented soy germ (SE5-OH tablets) | Soy isoflavones (daidzein) for people who make equol themselves |
|---|---|---|
| Absorption in people | Rapidly absorbed, plasma half-life about 8 hours, 82% excreted in urine; producer status did not change the pharmacokinetics.10 | Depends on gut bacteria; a 2015 review puts producers at about 50% of Asians and 25% of non-Asians.13 |
| GI tolerance | No serious adverse effects in 12-week to 1-year trials; one systemic rash at 30 mg/day.578 | See the soy isoflavones page.12 |
| Studied for | Hot flushes (B), mood (C), bone markers (C), wrinkles (C) | Menopausal symptoms, with benefit in producers only (C) |
- S-equol from fermented soy germ (SE5-OH tablets)
- Absorption in people
- Rapidly absorbed, plasma half-life about 8 hours, 82% excreted in urine; producer status did not change the pharmacokinetics.10
- GI tolerance
- No serious adverse effects in 12-week to 1-year trials; one systemic rash at 30 mg/day.578
- Studied for
- Hot flushes (B), mood (C), bone markers (C), wrinkles (C)
- Soy isoflavones (daidzein) for people who make equol themselves
What the human research says
Human trials only, one row per outcome. The form line shows what each trial actually tested. Grades follow our evidence-grading policy.
Trial map
11 graded outcomes, largest study first11 graded outcomes: 9 improved, 2 mixed. The largest, a 2019 meta-analysis of 728 people on hot flushes in postmenopausal women (pooled), found an improvement.
1Hot flushes in postmenopausal women (pooled)
Improved · Grade B · Meta-analysis, 728 people, 2019
Peri- or postmenopausal women in 5 randomized trials (6 trials, 779 women, reviewed)
Dose, result and source| Outcome | Found | People | Study | Who was studied |
|---|---|---|---|---|
| Hot flushes in postmenopausal women (pooled) | Improved | 728 | Grade B · Meta-analysis, 2019 | Peri- or postmenopausal women in 5 randomized trials (6 trials, 779 women, reviewed) |
| Hot flush frequency in equol non-producers | Improved | 160 | Grade B · RCT, 2012 | Equol non-producing postmenopausal Japanese women with at least 1 hot flush a day (126 completed) |
| Menopausal symptoms and mood | Improved | 134 | Grade C · RCT, 2009 | Japanese women aged 40 to 59 (34.3% equol producers) |
| Hot flash frequency vs soy isoflavones (active comparator) | Mixed | 102 | Grade C · RCT, 2012 | Postmenopausal women aged 45 to 65 with 5 or more hot flashes a day (US, per a 2015 review) |
| Hand osteoarthritis pain and function | Improved | 102 | Grade D · Open-label trial, 2025 | Japanese women aged 45 to 60 with hand osteoarthritis who did not make equol |
| Crow's-feet wrinkles | Improved | 101 | Grade C · RCT, 2012 | Equol non-producing postmenopausal Japanese women (pilot) |
| Menopausal symptoms with soy isoflavones, by equol producer status | Mixed | 96 | Grade C · RCT, 2008 | Healthy menopausal women, grouped as equol producers or non-producers after a week of isoflavones |
| Bone resorption and whole-body bone density | Improved | 93 | Grade C · RCT, 2011 | Non-equol-producing postmenopausal Japanese women (pilot) |
| Bone turnover markers and whole-body bone density (with resveratrol) | Improved | 60 | Grade C · RCT, 2023 | Healthy postmenopausal women (Italy); equol producer status not tested |
| Climacteric symptoms, skin AGEs and visceral fat | Improved | 57 | Grade C · RCT, 2021 | Postmenopausal Japanese women, mean age 56 (single centre) |
| HbA1c, LDL cholesterol and arterial stiffness in overweight adults | Improved | 54 | Grade C · Crossover RCT, 2013 | Overweight or obese Japanese outpatients (BMI 25 or more; 67.9% equol non-producers) |
Every graded row
11 rowsShowing 11 of 11 outcomes. Human trials only.
BGrade BHot flushes in postmenopausal women (pooled)Hot flushesLower hot flush scoresMeta-analysis · 5 studies
n 728 · 2019
Improved Equol significantly lowered hot flush scores overall, with a generally low risk of bias; two of the five pooled trials found no significant benefit and three did.
- Design
- Meta-analysis, 5 studies, n = 728, 2019
- Population
- Peri- or postmenopausal women in 5 randomized trials (6 trials, 779 women, reviewed)
- Form
- S-equol supplements, or soy isoflavones in equol producers
- Dose
- As given in each trial
- Duration
- Varied by trial
- Source
- Reference 4 · PubMed 30592686 (opens PubMed)
BGrade BHot flush frequency in equol non-producersHot flushes−58.7% vs −34.5% hot flushesRCT
n 160 · 2012
Improved Hot flushes fell by 1.9 a day (−58.7%) with S-equol vs 1.0 a day (−34.5%) with placebo (p = 0.009); hot flush severity and neck or shoulder stiffness also fell more. No serious adverse effects or changes in clinical parameters.
- Design
- RCT, n = 160, 2012
- Population
- Equol non-producing postmenopausal Japanese women with at least 1 hot flush a day (126 completed)
- Form
- Natural S-equol supplement vs placebo
- Dose
- 10 mg/day
- Duration
- 12 weeks
- Source
- Reference 5 · PubMed 21992596 (opens PubMed)
CGrade CMenopausal symptoms and moodMoodLower depression and fatigue scoresRCT
n 134 · 2009
Improved With 10 mg three times a day, depression scores fell versus placebo, as did tension-anxiety, depression-dejection and fatigue, while vigour rose. Equol non-producers after menopause improved from baseline on all symptom scores except depression. One woman had a systemic rash.
- Design
- RCT, n = 134, 2009
- Population
- Japanese women aged 40 to 59 (34.3% equol producers)
- Form
- S-equol supplement vs placebo
- Dose
- 10 mg once or three times a day
- Duration
- 12 weeks
- Source
- Reference 8 · PubMed 19131846 (opens PubMed)
CGrade CHot flash frequency vs soy isoflavones (active comparator)Hot flushesSimilar at week 8; 40 mg better cumulativelyRCT
n 102 · 2012
Mixed At week 8 hot flash frequency fell similarly in all groups. Over the whole 8 weeks, 40 mg/day reduced hot flashes more than isoflavones (p = 0.021), and 10 and 20 mg/day improved muscle and joint pain more than isoflavones.
- Design
- RCT, n = 102, 2012
- Population
- Postmenopausal women aged 45 to 65 with 5 or more hot flashes a day (US, per a 2015 review)
- Form
- S-equol (SE5-OH) 10, 20 or 40 mg/day vs soy isoflavones
- Dose
- 10, 20 or 40 mg/day
- Duration
- 8 weeks
- Source
- Reference 6 · PubMed 22409590 (opens PubMed)
CGrade CCrow's-feet wrinklesSkinSmaller wrinkle areaRCT
n 101 · 2012
Improved Wrinkle area fell significantly with both doses compared with placebo, and wrinkle depth with 30 mg/day. Hydration, water loss and elasticity did not change, and hormone and gynaecological checks were normal.
- Design
- RCT, n = 101, 2012
- Population
- Equol non-producing postmenopausal Japanese women (pilot)
- Form
- Natural S-equol 10 or 30 mg/day vs placebo
- Dose
- 10 or 30 mg/day
- Duration
- 12 weeks
- Source
- Reference 11 · PubMed 21934634 (opens PubMed)
CGrade CMenopausal symptoms with soy isoflavones, by equol producer statusHot flushesBenefit in producers onlyRCT
n 96 · 2008
Mixed Hot flashes and sweating improved at 3 months, and total symptoms at 6 months, only in women who produced equol; non-producers did not differ from placebo.
- Design
- RCT, n = 96, 2008
- Population
- Healthy menopausal women, grouped as equol producers or non-producers after a week of isoflavones
- Form
- Soy isoflavones 135 mg/day vs placebo (not an equol supplement)
- Dose
- 135 mg/day isoflavones
- Duration
- 6 months
- Source
- Reference 12 · PubMed 18395723 (opens PubMed)
CGrade CBone resorption and whole-body bone densityBone−23.94% vs −2.87% bone resorption markerRCT
n 93 · 2011
Improved With 10 mg/day, urinary deoxypyridinoline, a marker of bone breakdown, fell 23.94% vs 2.87% with placebo (P = 0.020), and whole-body bone density did not fall. Sex and thyroid hormones did not differ between groups.
- Design
- RCT, n = 93, 2011
- Population
- Non-equol-producing postmenopausal Japanese women (pilot)
- Form
- Natural S-equol supplement 2, 6 or 10 mg/day vs placebo
- Dose
- 2, 6 or 10 mg/day
- Duration
- 12 months
- Source
- Reference 7 · PubMed 21252728 (opens PubMed)
CGrade CBone turnover markers and whole-body bone density (with resveratrol)BoneBetter bone markers; higher whole-body BMDRCT
n 60 · 2023
Improved Deoxypyridinoline, osteocalcin and bone-specific alkaline phosphatase improved versus placebo (p < 0.0001 for all); TRACP-5b did not change significantly (p = 0.051). Whole-body bone density rose versus placebo (p = 0.022).
- Design
- RCT, n = 60, 2023
- Population
- Healthy postmenopausal women (Italy); equol producer status not tested
- Form
- 200 mg fermented soy supplying 10 mg equol, plus 25 mg resveratrol, vs placebo
- Dose
- 10 mg equol plus 25 mg resveratrol once daily
- Duration
- 12 months
- Source
- Reference 16 · PubMed 37569440 (opens PubMed)
CGrade CClimacteric symptoms, skin AGEs and visceral fatHot flushes81% vs 53% improvedRCT
n 57 · 2021
Improved Climacteric symptoms improved in 81% with equol vs 53% with control (p = 0.045). Metabolic and ageing biomarkers did not improve overall; skin autofluorescence and visceral fat improved in some subgroups, mainly equol producers.
- Design
- RCT, n = 57, 2021
- Population
- Postmenopausal Japanese women, mean age 56 (single centre)
- Form
- Equol-containing supplement vs control
- Dose
- Daily supplement (amount not stated in the abstract)
- Duration
- 3 months
- Source
- Reference 9 · PubMed 34506596 (opens PubMed)
CGrade CHbA1c, LDL cholesterol and arterial stiffness in overweight adultsMetabolicLower HbA1c, LDL-C and CAVICrossover RCT
n 54 · 2013
Improved Compared with placebo, S-equol significantly lowered HbA1c, LDL cholesterol and the cardio-ankle vascular index, with larger effects in women who were equol non-producers.
- Design
- Crossover RCT, n = 54, 2013
- Population
- Overweight or obese Japanese outpatients (BMI 25 or more; 67.9% equol non-producers)
- Form
- Natural S-equol tablets vs placebo (crossover, no washout)
- Dose
- 10 mg/day
- Duration
- 12 weeks per period
- Source
- Reference 15 · PubMed 22469418 (opens PubMed)
DGrade DHand osteoarthritis pain and functionJoint pain−34.0 mm pain on movementOpen-label trial
n 102 · 2025
Improved Pain on movement fell by 34.0 mm on a visual analogue scale and arm, shoulder and hand disability (DASH) scores fell by 6.6 points from baseline (both p < 0.001); improvement appeared within 1 to 3 months.
- Design
- Open-label trial, n = 102, 2025
- Population
- Japanese women aged 45 to 60 with hand osteoarthritis who did not make equol
- Form
- Natural S-equol supplement, no control group
- Dose
- 10 mg/day (two 2.5 mg tablets twice daily)
- Duration
- 12 weeks
- Source
- Reference 18 · PubMed 40666269 (opens PubMed)
What the numbers add up to
Each point is worked out from the data and the sources numbered on this page, with the arithmetic shown under it. It adds no new data and is not medical advice.
What the placebo did
In the largest trial, hot flushes fell 34.5% on placebo and 58.7% on S-equol, so about 24 percentage points of the fall belong to S-equol.5
How many people make equol
Studied doses
Doses used in research, shown against the official limits. They describe the studies, not a recommendation for you.
Studied doses in research, not advice. These are amounts used in research, not personal advice. Your clinician or pharmacist can say what fits you.
Doses studied in human trials
Doses studied in human trials ranged from 2 mg a day (bone pilot) to 40 mg a day (US hot flash pilot), with 10 mg a day used in most trials for 8 weeks to 1 year; one trial gave 10 mg three times a day. A 2015 review notes the 7- to 10-hour half-life, which is why some trials split the dose. These are research amounts, not product directions.76581310
When trials measured an effect
4 outcomes| Outcome | Measured at | Basis |
|---|---|---|
| Hot flushes | Measured at 8 to 12 weeks | Randomized trials in Japanese and US women56 |
| Bone resorption marker | Measured at 12 months | Pilot placebo-controlled trial7 |
| Hand osteoarthritis pain | Within 1 to 3 months | Single-arm 12-week pilot in 102 perimenopausal women18 |
| Blood S-equol after a dose | Half-life about 8 hours | Pharmacokinetic study in 12 postmenopausal women10 |
Interactions and safety
Published interactions only: each row cites a source. No row means none was found in our sources, not that a combination is safe.
What Equol meets
1 cited rowMedicines 1
Supplements and foods 0
No supplement rows in our sources.
- Measured in a human study
Choose a medicine or supplement above to read its cited rows here.
Also cited:
Breast cancer hormone therapy
PK studyMeasured in a human study
Breast cancer hormone therapy, for example anastrozole, letrozole, exemestane, tamoxifen: In 24 healthy postmenopausal women (6 per drug), an S-equol supplement at 10 mg/day for 7 days did not significantly change blood exposure (AUC) to any of the four drugs. Two authors were employees of the supplement's maker.
Source 17, Cancer Chemother Pharmacol (2025)
Interactions
1 agent| Agent | What the source says | Evidence |
|---|---|---|
| Medicines1 | ||
| Breast cancer hormone therapye.g. anastrozole, letrozole, exemestane, tamoxifen | In 24 healthy postmenopausal women (6 per drug), an S-equol supplement at 10 mg/day for 7 days did not significantly change blood exposure (AUC) to any of the four drugs. Two authors were employees of the supplement's maker.17 | PK study |
Check with what you take
Kept on this device onlyAdd what you take. We list every interaction our evidence profiles cite between Equol and your picks, and between your picks.
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Add a supplement or medicine you take to check it against Equol.
Starting from one medicine? The interaction checker rates how serious each pair is, on a curated list of 19 entries for 11 medicines. This cabinet has no severity rating: it lists every interaction row our supplement pages cite.
Who should be careful
4 groups- Hormone-sensitive conditions
- S-equol binds estrogen receptor beta. Trials checked hormones, endometrium and mammograms over 12 weeks to 1 year without finding problems, and a 2025 study found it did not significantly change blood levels of anastrozole, letrozole, exemestane or tamoxifen. None of the trials here reported on people with a history of hormone-sensitive cancer, who should ask their oncologist first.1011717
- Pregnancy and breastfeeding
- NCCIH says soy may be unsafe in pregnancy in amounts greater than those commonly found in foods, and little is known about such amounts while breastfeeding. LactMed has no equol entry, and the trials enrolled peri- and postmenopausal women and overweight adults; we found no data on S-equol supplements in pregnancy or breastfeeding.19415
- Soy allergy
- S-equol supplements are made by fermenting soy germ. NCCIH notes that some people are allergic to soy and that soy must be declared on US supplement labels; the hand osteoarthritis trial excluded people with soy allergy.191018
- People choosing a hot flash treatment
- The Menopause Society's 2023 statement lists equol as not recommended and names hormone therapy as the most effective treatment, with several recommended nonhormone options.2
How to read the label
What to check on the Supplement Facts panel.
How to read the label
2 checksS-equol, not isoflavones
Frequently asked questions
Short answers to common questions; the numbers link to the sources below.
Common questions
8 answersDoes S-equol help hot flashes?
Do I need equol if I already eat soy?
Is S-equol a hormone?
Is S-equol safe?
Can I take S-equol if I am allergic to soy?
Does S-equol interact with breast cancer drugs?
In a 2025 study of 24 postmenopausal women (6 per drug), 10 mg a day of S-equol for 7 days did not significantly change blood levels of anastrozole, letrozole, exemestane or tamoxifen. That study did not test whether it is safe after hormone-sensitive cancer, so ask an oncologist first.17
What is an equol producer?
Someone whose gut bacteria convert the soy isoflavone daidzein into S-equol. A 2015 review puts this at about 50% of Asians and 25% of non-Asians.13
Why does the Menopause Society not recommend equol?
Sources
18 sources: trial abstracts, NIH fact sheets and reference databases. Numbers in the text link here.
Sources cited on this page
18 sources- 1PubChem compound summary: (S)-equol (CID 91469)Database National Library of Medicine, 2026 · pubchem.ncbi.nlm.nih.gov
- 2The 2023 nonhormone therapy position statement of The North American Menopause Society.Guideline Menopause, 2023 · PMID 37252752
- 4Equol Decreases Hot Flashes in Postmenopausal Women: A Systematic Review and Meta-Analysis of Randomized Clinical Trials.Meta-analysis J Med Food, 2019 · PMID 30592686
- 5A natural S-equol supplement alleviates hot flushes and other menopausal symptoms in equol nonproducing postmenopausal Japanese women.RCT J Womens Health (Larchmt), 2012 · PMID 21992596
- 6A pilot study on the effects of S-equol compared to soy isoflavones on menopausal hot flash frequency.RCT J Womens Health (Larchmt), 2012 · PMID 22409590
- 7Natural S-equol decreases bone resorption in postmenopausal, non-equol-producing Japanese women: a pilot randomized, placebo-controlled trial.RCT Menopause, 2011 · PMID 21252728
- 8New equol supplement for relieving menopausal symptoms: randomized, placebo-controlled trial of Japanese women.RCT Menopause, 2009 · PMID 19131846
- 9Effects of an equol-containing supplement on advanced glycation end products, visceral fat and climacteric symptoms in postmenopausal women: A randomized controlled trial.RCT PLoS One, 2021 · PMID 34506596
- 10The pharmacokinetics of S-(-)equol administered as SE5-OH tablets to healthy postmenopausal women.PK study J Nutr, 2009 · PMID 19776178
- 11The effects of natural S-equol supplementation on skin aging in postmenopausal women: a pilot randomized placebo-controlled trial.RCT Menopause, 2012 · PMID 21934634
- 12Effect of intestinal production of equol on menopausal symptoms in women treated with soy isoflavones.RCT Int J Gynaecol Obstet, 2008 · PMID 18395723
- 13S-equol: a potential nonhormonal agent for menopause-related symptom relief.Review J Womens Health (Larchmt), 2015 · PMID 25692726
- 14Acute and subchronic toxicity and genotoxicity of SE5-OH, an equol-rich product produced by Lactococcus garvieae.Animal study Food Chem Toxicol, 2008 · PMID 18554770
- 15Effects of natural S-equol supplements on overweight or obesity and metabolic syndrome in the Japanese, based on sex and equol status.Crossover RCT Clin Endocrinol (Oxf), 2013 · PMID 22469418
- 16Equol and Resveratrol Improve Bone Turnover Biomarkers in Postmenopausal Women: A Clinical Trial.RCT Int J Mol Sci, 2023 · PMID 37569440
- 17Lack of effects of S-equol-containing supplement on the pharmacokinetics of oral hormone therapy drugs for breast cancer.PK study Cancer Chemother Pharmacol, 2025 · PMID 41359041
- 18Effects of Equol on Hand Osteoarthritis in Perimenopausal Women: A Pilot Study.Open-label trial Cureus, 2025 · PMID 40666269
- 19Soy: Usefulness and SafetyFact sheet National Center for Complementary and Integrative Health (NCCIH), 2025 · nccih.nih.gov
What changed
Every dated change to this page: what changed, who made it and why.
Change log
2 entries| Date | Change | Who and why |
|---|---|---|
| key facts, evidence, interactions, who should avoid, time to effect, FAQ, questions, related | Added a 2025 pharmacokinetic study showing S-equol 10 mg/day did not change blood levels of anastrozole, letrozole, exemestane or tamoxifen (first interaction row); a 12-month equol-plus-resveratrol bone trial (60 women, grade C, combination product); and a 12-week single-arm hand osteoarthritis pilot (102 women, grade D, maker-sponsored) with its time to effect. Pregnancy and breastfeeding now cite NCCIH's soy page (April 2025); added a soy allergy note. Trimmed the FAQ from 10 to 8 by removing items that repeat the page's own questions (bones, skin, mood, studied dose) and adding drug interactions and soy allergy; added page questions and goal-hub links. Searched PubMed for 2020–2026 equol meta-analyses and RCTs: no newer hot flush meta-analysis than 2019; a 2026 premenstrual symptoms RCT (PMID 42528239) has no abstract on PubMed and was not added. LactMed and LiverTox have no equol or soy isoflavone entry. | Writer: Kymata Health EditorialTrigger: A–Z audit against docs/supplements/AUDIT-STANDARD.md |
| all | New page. Every PMID checked with NCBI E-utilities (esummary title, year and journal) and its abstract read with efetch; PubChem read on the date shown. The rat toxicology study is cited only for the production method in the mechanism section. | Writer: Kymata Health EditorialTrigger: new page |
Supplement & Nutrient Encyclopedia. Educational information only; it is not medical advice and does not replace a clinician. Dietary supplements are not intended to diagnose, treat, cure or prevent any disease. Statements about supplements have not been evaluated by the FDA.