Swanson Alpha Lipoic Acid 600mg capsules — antioxidant supplement available in Ireland with delivery from Dublin

Alpha Lipoic Acid Supplement Ireland: Evidence Guide 2026

Evidence Guide · Alpha Lipoic Acid · Ireland · June 2026

Alpha lipoic acid (ALA) is one of the most researched antioxidant compounds in nutritional science — with a particularly strong evidence base in peripheral neuropathy. This guide covers what the evidence actually shows, what it does not, and what to look for in an Irish supplement.

At a Glance

Alpha lipoic acid (ALA) is a naturally occurring organosulfur antioxidant synthesised in every human cell and found in small amounts in food. In Ireland, it is classified as a food supplement under FSAI guidelines — it is not a medicine, not a drug, and no EU-authorised health claim under EC Regulation 1924/2006 currently applies to it. The strongest human evidence relates to diabetic peripheral neuropathy: the ALADIN trial (Ziegler et al., Diabetologia, 1995, PMID 8786016) established IV ALA's effect, and the SYDNEY 2 trial (Ziegler et al., Diabetes Care, 2006, PMID 17065669) confirmed that 600mg/day oral ALA significantly reduced neuropathy symptom scores vs placebo (p<0.001) in 181 participants. Longer-term systematic evidence is less certain — a 2024 Cochrane review found ALA probably has little to no effect on neuropathy symptoms at 6 months. ALA is not proven to treat or prevent any disease. Swanson Alpha Lipoic Acid 600mg (60 gelatin capsules, €24.95 inc. 13.5% Irish VAT) is available with 1–2 business day tracked delivery from Dublin.

Alpha lipoic acid (ALA, lipoic acid) definition: Alpha lipoic acid is a naturally occurring organosulfur compound produced endogenously in human mitochondria from octanoic acid, functioning as an essential cofactor in oxidative metabolism and classified as both a fat-soluble and water-soluble antioxidant found in trace quantities in organ meats, red meat, spinach, and broccoli.

What is an alpha lipoic acid supplement in Ireland?

An alpha lipoic acid supplement in Ireland is a food supplement — typically a 300mg to 600mg capsule — providing concentrated ALA beyond what food sources supply (dietary intake is estimated at 1–6mg/day). ALA supplements are regulated by the Food Safety Authority of Ireland (FSAI) as food supplements, not medicines. ALA is not a stimulant, not a hormone, and not a prescription drug. The strongest short-term human evidence is in diabetic peripheral neuropathy at 600mg/day (SYDNEY 2, Ziegler et al., Diabetes Care, 2006, PMID 17065669); longer-term Cochrane review evidence (2024) is less certain. Evidence for general antioxidant, blood sugar, or weight management benefits in healthy adults is more limited. Swanson Alpha Lipoic Acid 600mg (€24.95) ships from Dublin with 1–2 business day tracked delivery nationwide.

Research Context — Not Product Claims

The clinical research discussed in this article relates to alpha lipoic acid as a studied compound. It should not be read as a claim that Swanson Alpha Lipoic Acid 600mg produces these effects. This product is a food supplement, not a medicine. No authorised EU health claim is currently made for alpha lipoic acid on this page or on the product.

Available Now · Ships from Dublin

Swanson Alpha Lipoic Acid 600mg — 60 Capsules

High-dose ALA supplement, 600mg per capsule. Non-GMO. Manufactured under GMP standards by Swanson Health. The dose used in most major human ALA trials.

600mg per capsule 60 capsules Non-GMO GMP manufactured By Swanson Health Not a medicine
✓ Buy Now — €24.95

Probiotic.ie · Authorised Irish retailer for Swanson · Ships from Dublin · 1–2 business day tracked delivery · Free over €75 · Irish VAT 13.5% included · Not a medicine · Regulated under FSAI food supplement guidelines

Fast Facts — Alpha Lipoic Acid
  • What it is: Organosulfur antioxidant compound, both fat- and water-soluble
  • Also known as: ALA, lipoic acid, thioctic acid
  • Produced in the body: Yes — synthesised in mitochondria from octanoic acid
  • Dietary sources: Kidney, heart, red meat, spinach, broccoli (trace amounts; ~1–6mg/day from food)
  • Supplement form: Synthetic racemic mix of R-ALA + S-ALA (50:50); also available as R-ALA only
  • Typical trial dose: 300–600mg/day oral — clinical trials have used up to 1,800mg/day IV
  • EFSA position: No Dietary Reference Value established; no authorised EU health claim
  • Is it a stimulant? No. ALA has no stimulant properties.
  • Is it a medicine? No. In Ireland, it is a food supplement regulated by FSAI.
  • Capsule type (Swanson 600mg): Gelatin — not suitable for vegans or vegetarians
  • Irish regulatory status: Food supplement under FSAI guidelines — not a medicine
  • Irish VAT rate on supplements: 13.5%
What Alpha Lipoic Acid Is Not
  • Alpha lipoic acid is not a medicine or licensed drug in Ireland
  • Alpha lipoic acid is not proven to treat or prevent diabetes in humans
  • Alpha lipoic acid is not proven to extend human lifespan
  • Alpha lipoic acid is not a weight loss drug — modest effects in one RCT, not replicated at scale
  • Alpha lipoic acid is not the same as alpha linolenic acid (ALA also = the omega-3 precursor — a different compound)
  • Alpha lipoic acid is not a stimulant and does not affect energy levels directly
  • Alpha lipoic acid is not authorised under any EU health claim on this product
Evidence Summary

What is well-supported: Improvements in diabetic peripheral neuropathy symptom scores with 600mg/day oral ALA — multiple RCTs including SYDNEY 2 (Ziegler et al., Diabetes Care, 2006, PMID 17065669, n=181, p<0.001 vs placebo).

What is not proven: Human RCT evidence for ALA in general antioxidant protection, blood sugar control in non-diabetics, weight management, or skin improvement in healthy adults is limited and inconsistent.

Most relevant human dose range: 300–600mg/day oral (consistent across major neuropathy and blood sugar trials).

Key safety note: Risk of hypoglycaemia if combined with insulin or oral blood-glucose-lowering agents. Thyroid medication interaction possible. Consult GP if on any medication.

Feature Specification Evidence Level
Compound type Organosulfur antioxidant — fat- and water-soluble Established
Endogenous production Yes — mitochondrial cofactor synthesised from octanoic acid Established
Dietary sources Organ meats, red meat, spinach, broccoli (~1–6mg/day) Established
Diabetic neuropathy (600mg/day) Significant symptom reduction — SYDNEY 2 RCT, n=181 Strong RCT evidence
Blood sugar / insulin sensitivity Mechanistically plausible; human trial results mixed Mixed RCT
Weight management One RCT showed modest effect; not replicated at scale Limited
Skin antioxidant / photoprotection Preclinical and small trials only in healthy adults Preclinical / Limited
Longevity / lifespan extension No human evidence Not established in humans
Vegetarian / vegan suitability (Swanson 600mg) No — gelatin capsule Confirmed
Irish regulatory status FSAI food supplement — not a medicine Confirmed
Irish VAT rate 13.5% Confirmed
Compound Overview

What is alpha lipoic acid?

Alpha lipoic acid (ALA) — also called lipoic acid or thioctic acid — is a sulphur-containing fatty acid that plays a central role in mitochondrial energy metabolism. Every cell in the human body produces it in small amounts. Its primary biochemical job is to act as a cofactor in multi-enzyme complexes that convert glucose into usable energy (ATP) — specifically the pyruvate dehydrogenase and alpha-ketoglutarate dehydrogenase complexes.[1]

What sets ALA apart from most other antioxidants is its dual solubility. Most antioxidants work either in fat-soluble environments (like vitamin E in cell membranes) or water-soluble environments (like vitamin C in plasma). ALA works in both — meaning it can reach and act in a wider range of cellular and tissue environments than most compounds.[2]

ALA also has the ability to regenerate other antioxidants — including glutathione, vitamin C, and vitamin E — after they have been oxidised, which has made it a subject of significant research interest in metabolic and neurological conditions.[3]

600mg
Daily dose used in SYDNEY 2 RCT (Ziegler et al., 2006)
181
Participants in SYDNEY 2 trial — largest oral ALA neuropathy RCT
1–6mg
Estimated daily ALA from food sources (Shay et al., 2009)
2
Number of forms: R-ALA (natural) + S-ALA (synthetic) in racemic supplements
Mitochondrial Cofactor
ALA is an essential cofactor in the pyruvate dehydrogenase complex, which converts glucose-derived pyruvate into acetyl-CoA for entry into the Krebs cycle. This is established biochemistry — not a supplement claim.
Evidence: Established biochemically
🛡️
Direct Radical Scavenging
ALA is proposed to directly neutralise reactive oxygen species (ROS) including superoxide, hydroxyl radicals, and hypochlorous acid in both aqueous and lipid environments due to its dual solubility.
Evidence: Established in vitro; supported by human biomarker data
🔄
Antioxidant Recycling
ALA is proposed to regenerate oxidised glutathione, vitamin C, and vitamin E — extending their effective activity. This "antioxidant network" theory is well-established in cell models but harder to measure clinically in humans.
Evidence: Strong in vitro; limited direct human RCT evidence
🍬
Glucose Uptake (GLUT4)
ALA is proposed to activate GLUT4 transporter translocation to the cell membrane, increasing glucose uptake in muscle cells. This mechanism underlies its study in insulin sensitivity and diabetic neuropathy contexts.
Evidence: Animal models + small human trials; mechanism plausible
🧠
Neuroprotective Potential
In peripheral nerve tissue, ALA is proposed to reduce oxidative stress-driven nerve damage — the mechanism studied in diabetic neuropathy RCTs. Preclinical models suggest benefit in neuroinflammation and MS contexts; human evidence is limited outside diabetes.
Evidence: RCTs in diabetic neuropathy; preclinical for other conditions
🧬
Chelation of Metal Ions
ALA is proposed to chelate pro-oxidant metal ions including iron and copper, which can catalyse free radical production. This is thought to contribute to its protective effects in heavy metal exposure — including mercury — though evidence in humans is limited.
Evidence: In vitro; limited human data
Dietary Sources

Alpha lipoic acid in food — natural sources

Alpha lipoic acid is found in a wide range of foods but always in small quantities. Dietary intake from normal food is estimated at approximately 1–6mg per day.[3] The richest sources are organ meats — particularly kidney and heart — which reflects ALA's role as a mitochondrial cofactor. Tissues with high metabolic activity contain more mitochondria and therefore more ALA.

Among plant foods, spinach and broccoli are the most studied sources, with tomatoes, Brussels sprouts, and garden peas also containing detectable amounts. The key point: food sources provide nowhere near the 300–600mg doses used in clinical trials. Supplementation is used specifically when higher amounts are sought.

Food Source Category ALA Content (approximate) Relative Richness
Kidney (beef/pork) Organ meat Highest — exact figures vary by study Richest source
Heart (beef) Organ meat High Very rich
Red meat (beef, lamb) Meat Moderate Good source
Spinach Leafy vegetable Low-moderate Best plant source
Broccoli Vegetable Low-moderate Good plant source
Tomatoes Vegetable Low Minor source
Brussels sprouts Vegetable Low Minor source
Garden peas Legume Trace Trace amounts
Key Context

Even a diet rich in spinach and red meat is estimated to provide no more than 6mg of alpha lipoic acid per day. Clinical trials studying ALA's effects on neuropathy and blood sugar use 300–600mg/day — 50 to 100 times more than food alone can realistically provide. This gap is why oral supplementation is used when higher intakes are sought.

Mechanism of Action

How alpha lipoic acid works — antioxidant mechanisms

ALA's antioxidant function operates through three interconnected pathways. First, it directly neutralises reactive oxygen species (ROS) — the unstable molecules that damage cells, proteins, and DNA when produced in excess. Second, it regenerates other depleted antioxidants — glutathione, vitamin C, and vitamin E — effectively extending their activity. Third, in its reduced form (dihydrolipoic acid, or DHLA), it is itself a potent antioxidant with direct scavenging activity.[2]

The glutathione connection is particularly relevant. Glutathione is the body's primary intracellular antioxidant, and low glutathione levels are associated with numerous chronic disease states. ALA is proposed to increase intracellular glutathione by donating cysteine (a precursor to glutathione synthesis) and by directly reducing oxidised glutathione back to its active form. This is why ALA is often combined with N-acetyl cysteine (NAC) in research contexts — both support glutathione availability through different mechanisms.[3]

ALA is also studied in the context of mitochondrial function and the AMPK energy-sensing pathway. In animal models and cell studies, ALA has been shown to activate AMPK — an enzyme that regulates cellular energy balance and is a target in type 2 diabetes research. Whether this translates meaningfully to humans at oral supplement doses remains an active area of research.

Evidence Firewall

The mechanisms above are established in biochemical and preclinical research. Where mechanism research in cell or animal models has not been confirmed in human RCTs — particularly for AMPK activation, weight management, and longevity — this article uses hedged language. The SYDNEY 2 RCT data on neuropathy is the strongest human evidence base for ALA; other applications remain more speculative.

Clinical Evidence

Neuropathy and blood sugar — what the evidence shows

Alpha lipoic acid has the most substantial human clinical trial evidence of any antioxidant supplement studied in the context of diabetic peripheral neuropathy. The evidence base spans three decades of RCTs.

The ALADIN trial (Ziegler et al., Deutsche Klinik für Diagnostik, Diabetologia, 1995, PMID 8786016) was one of the first major RCTs — using intravenous ALA at 600mg/day over 3 weeks in participants with symptomatic diabetic neuropathy. IV ALA produced significant reductions in the Neuropathy Symptom Score vs placebo. The SYDNEY 2 trial (Ziegler et al., Diabetes Care, 2006, PMID 17065669) was the pivotal oral ALA study — 181 participants, 600mg/day oral, 5 weeks. Total Symptom Score improvements were statistically significant vs placebo (p<0.001).[4]

RCT
SYDNEY 2 Trial — Oral ALA in Diabetic Neuropathy (Ziegler et al., 2006)
Population: 181 adults with type 2 diabetes and symptomatic peripheral neuropathy. Intervention: 600mg/day oral ALA vs placebo for 5 weeks. Outcome: Significant reduction in Total Symptom Score (pain, burning, paraesthesia, numbness) — p<0.001 vs placebo. Number needed to treat (NNT) to achieve meaningful improvement: approximately 5.1. Conclusion: 600mg/day oral ALA is effective for symptomatic relief of diabetic neuropathy over 5 weeks. No serious adverse events reported.

Ziegler D et al. Oral treatment with alpha-lipoic acid improves symptomatic diabetic polyneuropathy: the SYDNEY 2 trial. Diabetes Care. 2006;29(11):2365–2370. PMID 17065669.
Meta-Analysis
Systematic Review of ALA in Diabetic Neuropathy — Confirmatory
Multiple systematic reviews of ALA neuropathy trials have concluded that 600mg/day oral ALA consistently outperforms placebo in reducing neuropathic symptoms in diabetic populations. The evidence is considered sufficiently robust that ALA is used in this context in some European clinical settings. The key limitation: all major RCTs are in diabetic populations — evidence for ALA in non-diabetic neuropathy is far more limited.

Packer L, Kraemer K, Rimbach G. Molecular aspects of lipoic acid in the prevention of diabetes complications. Nutrition. 2001;17(10):888–895. PMID 11684407.
Mixed RCT
ALA and Insulin Sensitivity / Blood Sugar — Mixed Results
Several small RCTs have examined ALA's effect on insulin sensitivity and blood glucose in type 2 diabetes. Mechanistically, ALA is proposed to activate GLUT4 glucose transporters in muscle cells, improving glucose uptake. Some trials have shown modest improvements in fasting glucose and insulin sensitivity markers. However, results are inconsistent across studies, doses, and populations. A 2011 RCT (Koh et al., Am J Med, PMID 21187184) testing ALA for weight in obese subjects found modest but significant weight reduction at high doses — but this has not been replicated at scale in healthy adults.

Koh EH et al. Effects of alpha-lipoic acid on body weight in obese subjects. Am J Med. 2011;124(1):85.e1-8. PMID 21187184.
Observational / Preclinical
ALA and Multiple Sclerosis — Early Research Only
Alpha lipoic acid has been studied in the context of multiple sclerosis based on its anti-inflammatory and neuroprotective properties. Yadav et al. (Oregon Health and Science University, Neurotherapeutics, 2010, PMID 20880501) reviewed preclinical and early human data, noting that ALA reduced matrix metalloproteinase-9 (MMP-9) levels in a small MS trial. This is preliminary evidence only — no large RCT has established ALA as effective for MS, and it is not used clinically for this purpose in Ireland.

Yadav V et al. Lipoic acid in inflammatory and degenerative neurological conditions. Neurotherapeutics. 2010;7(4):411–418. PMID 20880501.
Cochrane Review 2024
Longer-Term Evidence Less Certain — Cochrane Systematic Review Caveat
A 2024 Cochrane systematic review of ALA in diabetic neuropathy concluded that while short-term RCTs (4–5 weeks) show symptom improvements, ALA compared with placebo probably has little to no effect on neuropathy symptoms at 6 months. The certainty of evidence was rated as moderate to low. This does not invalidate the short-term RCT findings — it reflects a genuine gap in long-term trial data. For anyone considering ALA supplementation in the context of neuropathy, this balance of evidence is important context: short-term signals exist, but longer-term benefit has not been established.

Mijnhout GS et al. Alpha lipoic acid for symptomatic peripheral neuropathy. Cochrane Database Syst Rev. 2024. [Cochrane systematic review — see Cochrane Library for current version.]
Limitation
Evidence Gap — Healthy Adults Without Neuropathy or Diabetes
The majority of high-quality ALA RCT evidence is in populations with diabetic neuropathy. For healthy adults without these conditions, the evidence base for meaningful benefit from ALA supplementation is thin. General antioxidant supplementation in healthy adults has not shown consistent benefit in large trials. ALA may support cellular antioxidant capacity, but whether this translates to measurable health outcomes in a non-disease population has not been established. This is not unique to ALA — it reflects the general challenge in nutraceutical research.
Forms of ALA

R-alpha lipoic acid vs alpha lipoic acid — which is better?

This is one of the most common questions about ALA supplementation. It matters because ALA exists in two mirror-image molecular forms (enantiomers): R-ALA and S-ALA. Standard synthetic ALA supplements — including Swanson's — contain a 50:50 racemic mix of both. R-ALA-only supplements also exist.

R-ALA is the form produced naturally in the human body and the form that functions as a mitochondrial cofactor. It is considered the biologically active enantiomer. S-ALA is the synthetic mirror image — not produced in the body and thought to have lower enzymatic activity. The argument for R-ALA supplements is that you get more of the active form per milligram.

The counterargument: every major human RCT showing benefit in diabetic neuropathy — including SYDNEY 2 — used standard racemic ALA (50:50 mix), not pure R-ALA. So the evidence base exists for racemic ALA, not for pure R-ALA. Additionally, R-ALA is significantly less stable than racemic ALA — it degrades more rapidly at room temperature, which affects shelf life and quality.[3]

Factor Standard ALA (Racemic) R-ALA Only
Composition 50% R-ALA + 50% S-ALA 100% R-ALA
Biological activity Moderate — R-ALA fraction is active Higher per mg
Human RCT evidence base Strong (SYDNEY 2, ALADIN, multiple RCTs) Minimal — no large RCTs
Stability / shelf life Stable Less stable — degrades faster
Cost Lower Significantly higher
Recommended for general supplementation Yes — evidence-backed dose Possibly — but less studied
Practical Summary

For most people seeking ALA supplementation, standard racemic ALA at 600mg/day is the evidence-backed choice — it is what the major human trials used. R-ALA is theoretically more active per milligram, but no head-to-head human RCT has confirmed this translates to better clinical outcomes. If choosing R-ALA, ensure it is sodium-bound (sodium R-lipoate) for improved stability.

Dosage & Safety

Alpha lipoic acid dosage, timing, and safety

The dose range used across major human trials is 300–600mg/day oral. SYDNEY 2 and several other key RCTs used 600mg/day. Some IV trials used up to 600mg/day intravenously, which has significantly higher bioavailability than oral administration. EFSA has not established a Dietary Reference Value or tolerable upper intake level for ALA as a supplement — dosing guidance is based on clinical trial data.[4]

Timing: ALA is better absorbed on an empty stomach — food can reduce absorption by up to 50% in some studies. However, gastrointestinal side effects (nausea, stomach discomfort) are more common on an empty stomach. Taking ALA 30 minutes before a meal is a practical middle ground. Swanson's label recommends taking with food and water to minimise GI discomfort, which is the safer approach for most people.

Safety and interactions

ALA has a strong safety record at 300–600mg/day in clinical trials, including multi-year use. Key safety considerations:

Safety Consideration Details Risk Level
Diabetes medication interaction ALA may enhance blood glucose lowering — risk of hypoglycaemia if combined with insulin or oral hypoglycaemics Consult GP — important
Thyroid medication ALA may interfere with T4 to T3 conversion — possible interaction with levothyroxine Monitor — discuss with GP
Thiamine (B1) deficiency High-dose ALA may exacerbate B1 deficiency in at-risk individuals (e.g. heavy alcohol use) Avoid without B1 supplementation
Pregnancy / breastfeeding Safety data insufficient — not recommended unless directed by a doctor Avoid unless prescribed
GI discomfort (nausea) Most common side effect — usually mild and dose-dependent Take with food to reduce
Skin rash Reported rarely — likely allergic response; discontinue if occurs Rare
Healthy adults (300–600mg) No serious adverse events in major RCTs at standard doses Generally well tolerated
Days 1–3
Initial adjustment — some people experience mild nausea, particularly if taken on an empty stomach. Take with a small meal if this occurs.
Weeks 1–2
Absorption and tissue distribution occurs over the first weeks. Based on trial data, measurable antioxidant biomarker changes are typically detectable in this window.
Weeks 3–5
The SYDNEY 2 trial observed statistically significant symptom score changes vs placebo at 5 weeks in the diabetic neuropathy population. This is the relevant timeframe for the evidence-backed use case.
Long-term
ALA has been used in multi-year trials without serious safety signals. Whether long-term use in healthy adults confers meaningful benefit beyond the trial period has not been established.
Topical & Skin Research

Alpha lipoic acid for skin

ALA has gained attention in skincare and cosmetic applications due to its dual solubility — allowing it to penetrate both the aqueous and lipid layers of skin — and its proposed role as a topical antioxidant and photoprotective agent. ALA serums and creams have become mainstream in anti-ageing skincare ranges including The Ordinary.

The human evidence for topical or oral ALA specifically for skin improvement is modest. Preclinical studies have shown ALA can reduce UV-induced oxidative damage in skin cell models. A small human study found that topical 5% ALA cream reduced fine lines in photoaged skin, though the study was small and not replicated in large RCTs.[3]

For oral ALA supplementation and skin benefits in healthy adults, the evidence is currently insufficient to make specific claims. Any effect would be indirect — via systemic reduction of oxidative stress, which may slow skin oxidative damage over time. This is biologically plausible but not proven in large human trials.

What the evidence does not support

There is no evidence from large human RCTs that oral ALA supplementation produces measurable skin improvement in healthy adults. Skin antioxidant and anti-ageing claims for oral ALA supplements fall outside what the current evidence base can support. Topical ALA (in serums and creams) has separate, limited evidence for photoprotection in small studies.

Irish Market

Alpha lipoic acid in Ireland — regulatory status and where to buy

Alpha lipoic acid is a fully legal food supplement in Ireland. It is regulated by the Food Safety Authority of Ireland (FSAI) under EU food supplement legislation (Directive 2002/46/EC as transposed into Irish law). It is not a controlled substance, does not require a prescription, and is available over the counter and online. Irish VAT of 13.5% applies to food supplement sales.[8]

ALA may not be sold with disease treatment claims in Ireland. No EU-authorised health claim under EC Regulation 1924/2006 currently applies to alpha lipoic acid. Products marketed with claims to treat, prevent, or cure diabetic neuropathy, diabetes, or any other condition would fall under HPRA (Health Products Regulatory Authority) medicines regulation — a different regulatory framework requiring clinical authorisation that ALA supplements do not have.

Availability in Ireland has improved significantly. ALA supplements are stocked in health food stores and online. The most common doses available in Ireland are 300mg and 600mg capsules. Swanson's 600mg format is the dose used in the key SYDNEY 2 RCT.

Product Details Verified

Product details on this page — including dose (600mg per capsule), capsule count (60), form (gelatin capsule), and price (€24.95 inc. VAT at 13.5%) — were verified by Probiotic.ie from current Swanson Alpha Lipoic Acid 600mg product information. Product details should always be checked against the current label before use, as formulations and pricing may change.

Buying alpha lipoic acid in Ireland — comparison

Option Dose Capsules Vegan / Veg Price (approx.) Ships from Ireland Best suited for
Swanson ALA 600mg (Probiotic.ie) 600mg 60 No (gelatin) €24.95 Yes — Dublin, 1–2 days Adults seeking 600mg/day (SYDNEY 2 trial dose)
High-street pharmacy / health store (e.g. Holland & Barrett IE) Typically 200–300mg 30–60 Varies €15–€30+ In-store only or ship from UK Lower-dose general use
R-ALA only supplements (online) 100–300mg R-ALA 30–60 Varies €25–€50+ Usually UK/EU dispatch Those wanting pure R-form — less human RCT data
ALA + Acetyl-L-Carnitine combinations ALA typically 200mg 60–120 Varies €20–€40 Usually UK/EU dispatch Combination neuropathy research context
Why 600mg matters

The 600mg dose is clinically significant because it is the exact oral dose used in the SYDNEY 2 RCT — the largest and most-cited human trial of oral ALA in neuropathy. Many pharmacy and health store products supply 200–300mg. If you are seeking the evidence-aligned dose, 600mg is the relevant benchmark. Swanson Alpha Lipoic Acid 600mg delivers this in a single daily capsule.

Research Context — Not Product Claims

The clinical and mechanistic research discussed in this article relates to alpha lipoic acid as a studied compound. It should not be read as a claim that Swanson Alpha Lipoic Acid 600mg produces these effects. This product is a food supplement, not a medicine. No authorised EU health claim is currently made for alpha lipoic acid on this page or on the product.

In Stock · Ships from Dublin

Swanson Alpha Lipoic Acid 600mg — 60 Capsules

600mg per capsule. The dose used in the SYDNEY 2 RCT. Non-GMO. GMP manufactured by Swanson Health. Shipped from Dublin with 1–2 business day tracked delivery.

600mg ALA per capsule 60 capsules Non-GMO GMP manufactured By Swanson Health Ships from Dublin
✓ Buy Now — €24.95

Probiotic.ie · Authorised Irish retailer for Swanson · Ships from Dublin · 1–2 business day tracked delivery · Free delivery over €75 · Irish VAT 13.5% included · Not a medicine · FSAI-regulated food supplement

Key Facts — Alpha Lipoic Acid Ireland
  • Alpha lipoic acid (ALA) is a naturally occurring organosulfur antioxidant produced in human mitochondria and found in small amounts in organ meats, red meat, spinach, and broccoli.
  • ALA is not a medicine, stimulant, or hormone — it is a food supplement regulated by the FSAI in Ireland.
  • ALA is both fat-soluble and water-soluble — making it functional in a wider range of cellular environments than most single-solubility antioxidants.
  • The strongest human RCT evidence for ALA is in diabetic peripheral neuropathy: SYDNEY 2 (Ziegler et al., Diabetes Care, 2006, PMID 17065669) used 600mg/day oral ALA in 181 participants and showed significant Total Symptom Score reductions vs placebo (p<0.001).
  • Human trials for ALA in blood sugar, weight, and skin in healthy adults are more limited and show mixed results.
  • ALA is not proven to extend human lifespan or treat diabetes.
  • Dietary ALA from food is estimated at 1–6mg/day — far below the 300–600mg/day doses used in clinical trials.
  • Standard ALA supplements contain a 50:50 mix of R-ALA (the natural form) and S-ALA. All major human RCTs used this racemic mix — not R-ALA alone.
  • In Ireland, alpha lipoic acid supplements are regulated by FSAI as food supplements — not medicines. Irish VAT of 13.5% applies.
  • Swanson Alpha Lipoic Acid 600mg (60 gelatin capsules, €24.95 inc. 13.5% VAT) is available from Probiotic.ie with 1–2 business day tracked delivery from Dublin.
FAQ

Frequently asked questions — alpha lipoic acid Ireland

What is alpha lipoic acid?

Alpha lipoic acid (ALA) is a naturally occurring organosulfur compound found in every human cell, where it functions as a mitochondrial cofactor in energy metabolism. It is also a potent antioxidant — uniquely, it is both fat- and water-soluble, allowing it to act in a wide range of cellular environments. In Ireland, it is sold as a food supplement regulated by the FSAI. It is not a medicine.

What are the benefits of alpha lipoic acid?

The strongest human evidence for ALA relates to diabetic peripheral neuropathy, where the SYDNEY 2 RCT (Ziegler et al., Diabetes Care, 2006, PMID 17065669) showed significant symptom improvement with 600mg/day in 181 participants. ALA has also been studied for blood sugar metabolism, weight management, and skin antioxidant effects — but evidence in these areas, particularly in healthy adults, is more limited and inconsistent. No disease treatment claim is authorised for ALA as a food supplement in Ireland.

What is the recommended dosage of alpha lipoic acid?

Most human clinical trials use 300–600mg/day oral. SYDNEY 2 used 600mg/day. Swanson Alpha Lipoic Acid 600mg delivers one capsule per day. EFSA has not established a Dietary Reference Value for ALA. Always take with food and water; consult your GP if you take medication — particularly for diabetes or thyroid conditions.

What is the difference between R-alpha lipoic acid and alpha lipoic acid?

Standard ALA supplements contain a 50:50 synthetic mix of R-ALA and S-ALA (racemic ALA). R-ALA is the biologically active form produced naturally in the body. All major human RCTs — including SYDNEY 2 — used racemic ALA. R-ALA-only supplements exist but have less human trial evidence and are less stable at room temperature.

What are the side effects of alpha lipoic acid?

At 300–600mg/day, ALA is generally well tolerated. The most common side effects are gastrointestinal — nausea and stomach discomfort — particularly if taken on an empty stomach. Rare cases of skin rash have been reported. People with diabetes taking glucose-lowering medication should use caution due to a potential additive hypoglycaemic effect. Not recommended in pregnancy without medical supervision.

Is alpha lipoic acid safe?

ALA has been used in clinical trials at 300–600mg/day for up to 4 years without serious safety signals in healthy adults. Key interactions exist with diabetes medications (hypoglycaemia risk) and thyroid medication. Individuals with thiamine deficiency should not take high-dose ALA without medical guidance. For healthy adults at standard supplement doses, ALA is considered low-risk.

Is alpha lipoic acid legal in Ireland?

Yes. Alpha lipoic acid is a fully legal food supplement in Ireland, regulated by the Food Safety Authority of Ireland (FSAI) under EU food supplement legislation. It is not a controlled substance, does not require a prescription, and may be purchased over the counter or online. Irish VAT of 13.5% applies.

What foods contain alpha lipoic acid?

The richest dietary sources are organ meats (kidney, heart) and red meat. Plant sources include spinach, broccoli, tomatoes, and Brussels sprouts. However, total dietary ALA intake from food is estimated at only 1–6mg/day — far below the 300–600mg doses used in clinical trials. Supplementation provides a substantially higher concentration than diet alone.

Can alpha lipoic acid help with neuropathy?

In diabetic peripheral neuropathy specifically, multiple RCTs — including SYDNEY 2 (Ziegler et al., Diabetes Care, 2006, PMID 17065669) — have shown that 600mg/day oral ALA significantly reduces symptom scores compared to placebo. This is the most evidence-backed use of ALA. Evidence for ALA in non-diabetic neuropathy is much more limited. ALA is not licensed as a neuropathy treatment in Ireland and is classified as a food supplement only.

Where can I buy alpha lipoic acid in Ireland?

Swanson Alpha Lipoic Acid 600mg (60 capsules) is available from Probiotic.ie at €24.95 (Irish VAT 13.5% included), with 1–2 business day tracked delivery from Dublin. Free delivery applies on orders over €75. Probiotic.ie is an Irish-owned specialist supplement retailer regulated under FSAI food supplement guidelines.

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DG
Darren Grant — Founder, Probiotic.ie

Darren Grant is Managing Director of TenX Tech Ltd, the company behind Probiotic.ie and Probiotic.co.uk. He has operated FSAI-regulated supplement retail in Ireland since 2019, with a focus on evidence-led product selection and consumer education. All content is written to FSAI compliance standards and reviewed against current clinical evidence before publication.

Disclaimer: This guide is for educational purposes only and does not constitute medical advice. Swanson Alpha Lipoic Acid 600mg is a food supplement regulated under FSAI guidelines and is not intended to diagnose, treat, cure, or prevent any disease or medical condition. If you have persistent or worsening symptoms, consult a GP or relevant specialist. If you have diabetes, a thyroid condition, or take any regular medication, speak to your doctor before starting any supplement. Probiotic.ie is regulated under FSAI food supplement guidelines.

Sources
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  4. Ziegler D, Ametov A, Barinov A, et al. Oral treatment with alpha-lipoic acid improves symptomatic diabetic polyneuropathy: the SYDNEY 2 trial. Diabetes Care. 2006;29(11):2365–2370. PMID 17065669. — pubmed.ncbi.nlm.nih.gov/17065669
  5. Ziegler D, Hanefeld M, Ruhnau KJ, et al. Treatment of symptomatic diabetic peripheral neuropathy with the anti-oxidant alpha-lipoic acid: a 3-week multicentre randomized controlled trial (ALADIN Study). Diabetologia. 1995;38(12):1425–1433. PMID 8786016. — pubmed.ncbi.nlm.nih.gov/8786016
  6. Yadav V, Marracci G, Lovera J, et al. Lipoic acid in multiple sclerosis: a pilot study. Mult Scler. 2005;11(2):159–165. PMID 15794388. — pubmed.ncbi.nlm.nih.gov/15794388
  7. Koh EH, Lee WJ, Lee SA, et al. Effects of alpha-lipoic acid on body weight in obese subjects. Am J Med. 2011;124(1):85.e1-8. PMID 21187184. — pubmed.ncbi.nlm.nih.gov/21187184
  8. FSAI. Food Supplements Information Sheet. Food Safety Authority of Ireland. 2023. — fsai.ie/legislation/food-legislation/food-supplements