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Botanicals · Gummies

Mulberry Leaf

INCI: Mulberry Leaf (Morus alba leaf extract)

Mulberry leaf (Morus alba) is a botanical ingredient traditionally used in East Asian herbal systems. In private-label gummy manufacturing, it is positioned for glucose metabolism and sugar craving support. As a botanical on the EFSA on-hold list, it carries no authorised EU health claims under Reg. 432/2012; claim coverage is achieved through co-formulation with authorised nutrients such as Chromium or Inositol.

  • glucose-metabolism
  • sugar-craving-support
  • botanical-wellness
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Mulberry Leaf

At a glance

Definition
Mulberry leaf (Morus alba) is a botanical ingredient traditionally used in East Asian herbal systems. In private-label gummy manufacturing, it is positioned for glucose metabolism and sugar craving support. As a botanical on the EFSA on-hold list, it carries no authorised EU health claims under Reg. 432/2012; claim coverage is achieved through co-formulation with authorised nutrients such as Chromium or Inositol.
Common positionings
  • Glucose metabolism support
  • Post-meal glucose response
  • Sugar craving management
  • Metabolic wellness
  • Blood sugar balance support
Format suitability
Reviewed for gummies and sachets — confirmed per project.
Format & category fit

Where this ingredient fits in the DAT Supply catalogue

Every format chip links through to its manufacturing hub and to the private-label catalogue for that format. The category chip routes to the matching vertical hub on the categories index.

Positioning

What it is

Mulberry leaf is a botanical ingredient derived from the leaves of Morus alba, the white mulberry tree. It has a long history of use in traditional Chinese and Korean herbal medicine, primarily in the context of metabolic wellness and carbohydrate management. In modern dietary supplements, it is most commonly standardised to 1-deoxynojirimycin (DNJ), a compound that has been studied for its effect on post-meal glucose response.

Brands use mulberry leaf in gummy formats because it is heat-stable, soluble, and has a mild taste that works well in fruit-flavoured gummies. Its low cost tier makes it accessible for mass-market positioning, and it pairs effectively with other metabolic-support ingredients like Chromium and Inositol. As a botanical on the EFSA on-hold list, it cannot carry authorised health claims under Reg. 432/2012, but it remains one of the most familiar and commercially understood botanical actives for glucose metabolism support across EU and US markets.

Origin and history

White mulberry (Morus alba) is native to China and has been cultivated for thousands of years, primarily for silkworm rearing. The leaves have been used in traditional Chinese medicine for metabolic and digestive wellness, and the practice of using mulberry leaf tea for post-meal glucose management is well documented in East Asian herbal traditions. The tree was introduced to Europe and the Americas during the silk trade and has since naturalised in many temperate regions.

Industrial production of mulberry leaf extract involves harvesting the leaves, drying them, and extracting the active compounds—primarily DNJ—using water or ethanol. The extract is then standardised to a consistent DNJ content, typically around 1%, and spray-dried into a powder suitable for gummy and sachet manufacturing. The supply chain is well established, with major production in China, Korea, and Japan, and the ingredient is widely available at commodity pricing.

Scientific overview

The primary active compound in mulberry leaf is 1-deoxynojirimycin (DNJ), a polyhydroxylated piperidine alkaloid that acts as a competitive inhibitor of alpha-glucosidase enzymes in the small intestine. By slowing the breakdown of complex carbohydrates into absorbable monosaccharides, DNJ reduces the rate of glucose absorption after a meal, leading to a blunted postprandial glucose spike. This mechanism is well characterised in the scientific literature and is the basis for most commercial positioning of mulberry leaf supplements.

Bioavailability of DNJ is relatively low due to its hydrophilic nature, but the compound acts locally in the gut lumen, so systemic absorption is not required for its primary effect. Standardised extracts with 1% DNJ are the most common form used in supplements, though whole leaf powder is also available at a lower cost per serving. The ingredient is heat-stable and soluble, making it well suited for gummy manufacturing without significant degradation during processing.

Manufacturing watchpoints include ensuring consistent DNJ standardisation across batches, as the active content can vary with harvest season and processing method. The cost-per-mg is low, making mulberry leaf one of the more economical botanical actives for gummy formulations. However, brands should note that the onset of effect typically takes 2–3 weeks of consistent use, which should be reflected in consumer communication and product positioning.

Why brands use Mulberry Leaf

Mulberry leaf is one of the most familiar and commercially understood botanical actives for glucose metabolism support across EU and US markets. Its low cost tier and mild taste make it an attractive option for mass-market gummy ranges targeting metabolic wellness, sugar craving management, and post-meal glucose response. The ingredient pairs naturally with Chromium and Inositol, allowing brands to build comprehensive metabolic support formulations with multiple angles of claim coverage.

From a formulation and manufacturing perspective, mulberry leaf is heat-stable and soluble, which means it integrates cleanly into standard gummy production lines without requiring cold processing or encapsulation. The mild, slightly sweet taste is easy to mask with fruit flavours, and the ingredient does not cause the texture or stability issues that some other botanicals can introduce. The low cost tier also allows for flexible dosing within the 200–1500 mg range without significantly impacting per-unit cost.

For pack copy, brands should position mulberry leaf around general wellness and traditional use, or co-formulate with authorised nutrients for claim coverage. As a botanical on the EFSA on-hold list, no authorised health claims are available under Reg. 432/2012, so claim wording must come from co-formulated ingredients such as Chromium (contributes to normal macronutrient metabolism) or Inositol (contributes to normal insulin sensitivity). DAT reviews claim strategy, dosing, and formulation per project to ensure compliance with target market regulations.

Supported formats

Formats this ingredient is reviewed for

DAT Supply covers gummy, capsule, softgel, tablet, powder, oral strip, liquid drop, shot, jelly and pet formats. The list below reflects every format this ingredient is reviewed for — chips link through to the manufacturing hub for each format. Final compatibility, dose and matrix are confirmed per project.

Formulation notes

Verified formulation reference across the formats this ingredient is reviewed for — the Supported formats section lists every product format this active is approved for, and the per-format Considerations section below covers matrix-specific guidance. Final formulation, dose and on-pack copy are confirmed per project.

Gummy fit
Good
Heat stable
Yes
Soluble in matrix
Yes
Cost tier
Low

Forms available

  • Standardised leaf extract (typically 1% DNJ), whole leaf powder

Dosage reference

Typical brand positioning range is 200–1500 mg per serving. No EU NRV established as this is a botanical. DAT confirms dosing per project based on target market and claim strategy.

Taste & sensory

Mild, slightly sweet. Easy to mask in gummy formulations.

Manufacturing notes

Gummy-optimised dosing and format considerations apply. DAT confirms final formulation parameters per project.

Format considerations

Per-format formulation notes

Safe-baseline considerations for each format this ingredient is reviewed for. Final formulation, dose and on-pack copy are confirmed per project.

Gummies

  • Taste masking and aroma load against the cooked-base flavour — confirmed per project.
  • Heat exposure during cooking; coated or encapsulated forms may be required — confirmed per project.
  • Matrix choice (pectin vs gelatin) and its effect on ingredient stability — confirmed per project.
  • Per-gummy dose and serving count needed to hit the label claim — confirmed per project.

Develop in gummies →

Sachets

  • Powder flow and dose accuracy at single-serve sachet weights — confirmed per project.
  • Barrier requirements (oxygen, moisture) for the active — confirmed per project.
  • Reconstitution behaviour when the sachet is dosed into water — confirmed per project.

EU-authorised health claims

EU-authorised wording for this ingredient is reviewed per project against Reg. 1924/2006 and the authorised list under Reg. 432/2012. No final claim wording is implied by this page.

Authorised at ≥15% NRV per daily serving. Claim wording must appear verbatim on consumer packaging. DAT reviews final pack copy per project against EU 1924/2006 and the authorised list under EU 432/2012.

Mulberry leaf is a botanical ingredient on the EFSA on-hold list. No authorised health claims are available under Reg. (EU) 432/2012. Brands should position around general wellness and traditional use, or co-formulate with authorised-nutrient actives (e.g. Chromium, Inositol) for claim coverage. DAT reviews claim strategy per project.

Studies & evidence

External peer-reviewed sources and regulatory opinions. Citations only — DAT does not endorse the publishers.

  1. Kimura T, Nakagawa K, Kubota H, et al.·Journal of Agricultural and Food Chemistry·2007

  2. Hansawasdi C, Kawabata J·Fitoterapia·2006

  3. Lown M, Fuller R, Lightowler H, et al.·Nutrients·2017

  4. Asano N, Tomioka E, Kizu H, Matsui K·Carbohydrate Research·1994

  5. EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA)·EFSA Journal·2011

Catalogue match

Product concepts featuring Mulberry Leaf

Private-label product concepts where Mulberry Leaf appears in the formula. Each opens to a product brief and quote route.

Synergies & conflicts

Pairs well with

Pairs well with Chromium (glucose metabolism), Berberine (glucose metabolism), and Inositol (insulin signalling) for comprehensive metabolic support.

Care when combining with

Mild blood sugar effect. Safe for most populations. Onset of effect typically takes 2–3 weeks. DAT reviews per project for any contraindications.

Similar ingredients

Ingredients that frequently sit alongside this one in private-label supplement briefs.

Adjacent reading

Pairings, resource guides and blog notes most often associated with Mulberry Leaf on DAT Supply briefs.

Common pairings

Ingredients that frequently co-formulate with Mulberry Leaf.

Project handoff

Develop a formula featuring Mulberry Leaf

A ready white-label formula exists — open a product brief, or talk to our team to align the launch plan.

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