Tagatose (D-tagatose)

Also called D-tagatose, D-tagatose sweetener, Naturlose, tagatose sugar substitute, rare sugar tagatose.

The short answer

From 12 sources

Tagatose is a poorly absorbed sugar sold as a sweetener. Small trials found a single 5 g dose lowered post-drink glucose in people with raised blood sugar, and 45 g a day for 28 days did not enlarge the liver. At about 29 g in one go, bloating, gas and diarrhoea are common.

Key facts

What it is
Rare sugar related to fructose; poorly absorbed in the small intestine and fermented in the colon910
Blood sugar
A single 5 g dose lowered 2-hour glucose and glucose AUC in 33 adults with raised fasting glucose or type 2 diabetes, but not in 52 with normal glucose5
Gut effects
At 29 to 30 g in one dose, nausea (15.1%) and diarrhoea (31.5%) were reported in a 73-man screening study; flatulence was common910
Liver safety
45 g/day for 28 days in 12 men produced no change in liver volume or glycogen7
Regulatory
FDA has had no questions on GRAS notices GRN 78 (2001) and GRN 977 (2021); JECFA allocated an ADI "not specified"123

What it is

Tagatose is a rare sugar, a sibling of fructose, made from lactose or by enzymes and used as a low-calorie sweetener about 75 to 92% as sweet as table sugar.

How it works

Established

Tagatose is only partly absorbed in the small intestine. The unabsorbed portion draws water into the gut and is fermented in the large intestine, which explains the gas, distension and loose stools seen at higher doses. Effects on blood glucose in the trials are small and appear in people with raised glucose.5910

Forms

Form

The form on this page
FormElemental %Absorption (human data)GI toleranceStudied for
Tagatose powder or sweetener packetsVaries10Not applicable (sugar; labelled by grams per serving)Poorly absorbed in the small intestine; the remainder is fermented in the colon.10Dose-related nausea, bloating, flatulence and loose stools; most symptoms were light or moderate in a single 29 g dose study.910Post-drink glucose (5 to 10 g single doses), tolerance (29 to 30 g single doses), and 45 g/day for 28 days to 12 months

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

4 graded outcomes, largest study first

4 graded outcomes: 3 mixed, 1 no effect. The largest, a 2013 crossover trial of 85 people on blood glucose and insulin after a single drink, found mixed results.

1Blood glucose and insulin after a single drink

Mixed · Grade C · Crossover RCT, 85 people, 2013

Korean adults: 52 with normal glucose and 33 with impaired fasting glucose or newly diagnosed type 2 diabetes

Dose, result and source
Every graded outcome on this page, largest study first
OutcomeFoundPeopleStudyWho was studied
Blood glucose and insulin after a single drinkMixed85Grade C · Crossover RCT, 2013Korean adults: 52 with normal glucose and 33 with impaired fasting glucose or newly diagnosed type 2 diabetes
Food intake after a single doseMixed19Grade D · Crossover RCT, 200019 normal-weight men
Liver volume and glycogen (safety)No effect12Grade D · Crossover RCT, 200112 healthy men
Weight, HbA1c and HDL in type 2 diabetesMixed8Grade D · Open-label trial, 2010Adults with type 2 diabetes (pilot; 12 recruited, 8 analysed)
Each circle is one graded outcome on this page, numbered from the largest study down, and placed by how many people it studied (log scale). It shows who was studied and what was found, not advice about your dose.

Every graded row

4 rows

Showing 4 of 4 outcomes. Human trials only.

Mixed With 5 g, the hyperglycaemic group had lower glucose at 120 min (p = 0.019) and lower glucose AUC (p = 0.017); the normal group did not. With 10 g, normal-glucose adults had lower insulin at 30 and 60 min and lower insulin and C-peptide AUC. Age-matched groups responded similarly.

Design
Crossover RCT, n = 85, 2013
Population
Korean adults: 52 with normal glucose and 33 with impaired fasting glucose or newly diagnosed type 2 diabetes
Form
D-tagatose
Dose
5 g (hyperglycaemic group); 10 g (normal group, high dose)
Duration
Single dose per arm, 7 days apart
Source
Reference 5 · PubMed 23760573 (opens PubMed)

Mixed Energy intake at lunch and in the snacking period was similar to sucrose; at the supper buffet 9 h later it was 15% lower (P < 0.05). The authors link this to gut distension from unabsorbed tagatose.

Design
Crossover RCT, n = 19, 2000
Population
19 normal-weight men
Form
D-tagatose
Dose
29 g in a breakfast meal (replacing 29 g sucrose)
Duration
Single meal
Source
Reference 8 · PubMed 11029974 (opens PubMed)

No effect MR imaging and spectroscopy showed no treatment effect on liver volume or liver glycogen. Liver enzymes, uric acid and other clinical chemistry showed no clinically relevant changes.

Design
Crossover RCT, n = 12, 2001
Population
12 healthy men
Form
D-tagatose
Dose
15 g three times daily (45 g/day) replacing sucrose
Duration
28 days per arm
Source
Reference 7 · PubMed 11350207 (opens PubMed)

Mixed No serious adverse effects, but 10 of 12 recruited subjects had mild, transient GI side effects. Excluding 3 subjects whose diabetes medicines were changed, weight fell from 108.4 to 103.3 kg (P = 0.001); HbA1c fell non-significantly (10.6% to 9.6%, P = 0.08); HDL rose from 30.5 to 41.7 mg/dL in the 6 without lipid-drug changes.

Design
Open-label trial, n = 8, 2010
Population
Adults with type 2 diabetes (pilot; 12 recruited, 8 analysed)
Form
D-tagatose
Dose
15 g three times daily with food (45 g/day)
Duration
12 months after a 2-month run-in
Source
Reference 6 · PubMed 21147362 (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.

Safety was probed hard because rats' livers grew

High-dose tagatose caused reversible liver enlargement in rats, so researchers measured human liver volume and glycogen with MR after 28 days at 45 g a day and found no change.7

How we got this: Rationale and result of the 2001 MR liver study

The weight and HDL data are not strong

The one-year weight and HDL results come from 5 to 6 people after excluding others and had no placebo group, so they are a lead for larger trials, not an effect to expect.6

How we got this: Subset analysis in the 2010 pilot

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 single doses of 5 to 10 g for blood sugar and 29 to 30 g for tolerance up to 45 g a day (15 g three times daily) for 28 days in healthy men and for 12 months in 8 adults with type 2 diabetes. These are research doses, not advice.5679

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 Tagatose meets

2 cited rows

Medicines 1

Tagatose1 medicine · 1 supplement

Supplements and foods 1

  • Measured in a human study
  • Reference summary
Rows as our evidence profiles cite them; links stay on this site. Line weight shows what backs a row, not how serious an interaction is. No line means none was found in our sources, not that a combination is safe. Not medical advice: ask your pharmacist.

Interactions

2 agents
Published interactions, grouped by kind
AgentWhat the source saysEvidence
Medicines1
Glucose-lowering medicines (insulin, oral agents)A single 5 g dose lowered post-drink glucose in hyperglycaemic adults. No interaction trial with diabetes medicines was found, so an additive effect cannot be ruled out. In the 12-month pilot, three participants whose diabetes medicines changed were excluded from the weight analysis.56RCT
Other supplements1
Other poorly absorbed sugars and fibres (sugar alcohols, inulin)No study tested combinations. Each is fermented or osmotically active in the gut, so stacking them could add to gas and loose stools; this is an inference from the mechanism, not a trial finding.910Review

Check with what you take

Kept on this device only

Add what you take. We list every interaction our evidence profiles cite between Tagatose and your picks, and between your picks.

Most cited:

Add a supplement or medicine you take to check it against Tagatose.

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.

Not medical advice, and no dosing advice. An empty result means no row we cite names that pair, by name or through a drug class we can link the medicine to, not that a combination is safe. Where our sources name only a group of medicines we cannot match, the cabinet says so. Ask your pharmacist before you combine supplements and medicines.

Who should be careful

4 groups
Sensitive digestion
In a double-blind crossover, 29 g of tagatose scored higher than sucrose for rumbling, distension, nausea, flatulence and diarrhoea; two vomiting cases were recorded. The authors judged 30 g in one dose above what should be used for ordinary use.910
Diabetes on glucose-lowering medicines
Tagatose lowered glucose after a drink in hyperglycaemic adults. Anyone on insulin or other glucose-lowering drugs should ask their prescriber before regular use, since interaction trials are missing.56
Pregnancy, breastfeeding and children
No human trials in these groups were found in the sources reviewed, so the safety of regular supplemental intake is unknown.10
Labelling in Great Britain
UK authorisation requires the wording "excessive consumption may produce laxative effects" on foods above 15 g per serving and on beverages above 1% tagatose.4
Talk to your pharmacist or clinician before starting a supplement, especially if you take prescription medicines.

How to read the label

What to check on the Supplement Facts panel.

How to read the label

2 checks
Count grams per serving

Tagatose is sold as a sweetener, so the label usually lists grams per serving. The blood sugar result came from 5 g; gut symptoms were reported at 29 to 30 g.59

Watch for blends

Many sweeteners combine tagatose with other sugars or sugar alcohols. The trials here used tagatose alone, so their results do not carry over to blends.57

Label X-RayPhotograph a bottle's Supplement Facts panel and see each line, tagatose (D-tagatose) included, beside the doses and forms the trials used

Frequently asked questions

Short answers to common questions; the numbers link to the sources below.

Common questions

6 answers
What is tagatose?

A rare sugar related to fructose that is only partly absorbed. It is used as a low-calorie sweetener, about 75 to 92% as sweet as table sugar.1012

Does tagatose lower blood sugar?

After one 5 g drink it lowered 2-hour glucose in adults with raised fasting glucose or type 2 diabetes, not in adults with normal glucose. The evidence is a single small crossover trial.5

Is tagatose safe for the liver?

In 12 healthy men, 45 g a day for 28 days did not change liver volume, liver glycogen, liver enzymes or uric acid.7

Why does tagatose cause gas and diarrhoea?

Part of each dose is not absorbed. It holds water in the gut and is fermented in the colon, so doses around 29 to 30 g often caused bloating, flatulence and loose stools.910

Is tagatose regulated as safe?

FDA has had no questions on two GRAS notices (2001 and 2021), JECFA allocated an ADI "not specified", and it is an authorised novel food in Great Britain with a laxative-effect label statement above 15 g per serving.1234

Does tagatose help teeth?

A small trial found S. mutans fell only when chewing gum contained both tagatose and xylitol; neither alone reduced bacteria. The study had 19 volunteers.11

Sources

12 sources: trial abstracts, NIH fact sheets and reference databases. Numbers in the text link here.

Sources cited on this page

12 sources
  1. 1GRAS Notice GRN No. 78: D-Tagatose (FDA response: no questions, closed Oct 25, 2001)Database U.S. Food and Drug Administration, 2001 · hfpappexternal.fda.gov
  2. 2GRAS Notice GRN No. 977: D-tagatose produced via novel enzymatic cascade (FDA: no questions, closed Oct 21, 2021)Database U.S. Food and Drug Administration, 2021 · hfpappexternal.fda.gov
  3. 3D-tagatose: JECFA evaluation (ADI "not specified")Database WHO/FAO JECFA Food Additives database, 2004 · apps.who.int
  4. 4Authorised novel food NOVEL-40: D-Tagatose (Great Britain)Database UK Food Standards Agency, 2025 · data.food.gov.uk
  5. 5Beneficial effect of tagatose consumption on postprandial hyperglycemia in Koreans: a double-blind crossover designed study.Crossover RCT Food Funct, 2013 · PMID 23760573
  6. 6Dietary supplementation with d-tagatose in subjects with type 2 diabetes leads to weight loss and raises high-density lipoprotein cholesterol.Open-label trial Nutr Res, 2010 · PMID 21147362
  7. 7Effect of oral D-tagatose on liver volume and hepatic glycogen accumulation in healthy male volunteers.Crossover RCT Regul Toxicol Pharmacol, 2001 · PMID 11350207
  8. 8The acute effect of D-tagatose on food intake in human subjects.Crossover RCT Br J Nutr, 2000 · PMID 11029974
  9. 9Human tolerance to a single, high dose of D-tagatose.Crossover RCT Regul Toxicol Pharmacol, 1999 · PMID 10341163
  10. 10Human gastrointestinal tolerance to D-tagatose.Observational Regul Toxicol Pharmacol, 1999 · PMID 10341164
  11. 12Assessment of the Novel Food D-tagatose for a Change to the Conditions of Use (RP1652)Review UK Food Standards Agency, 2025 · science.food.gov.uk
  12. 11D-Tagatose Effectively Reduces the Number of Streptococcus mutans and Oral Bacteria in Healthy Adult Subjects: A Chewing Gum Pilot Study and Randomized Clinical Trial.RCT Acta Med Okayama, 2020 · PMID 32843762

What changed

Every dated change to this page: what changed, who made it and why.

Change log

2 entries
Dated changes to this page
DateChangeWho and why
evidenceAdversarial review: 12-man liver MR crossover regraded no-effect to D (too small to show no effect). Other rows match their abstracts; FDA GRAS records GRN 78 and GRN 977, the JECFA entry (ADI not specified, 2004) and the FSA NOVEL-40 labelling condition re-opened and confirmed.Writer: Kymata Health EditorialTrigger: adversarial review
allInitial editorial evidence review. Every PMID checked against NCBI E-utilities esummary (title, year, journal) and each cited abstract read; figures taken from the abstracts. Regulatory status from the FDA GRAS inventory (GRN 78, GRN 977), the WHO/FAO JECFA database and the UK FSA novel food register.Writer: Kymata Health EditorialTrigger: new page

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