Sweet Woodruff (Galium odoratum)

Galium odoratum (syn. Asperula odorata)
Evidence Level
Preliminary
3 Clinical Trials
6 Documented Benefits
1/5 Evidence Score

Sweet woodruff (Galium odoratum, also listed as Asperula odorata) is a low woodland herb of the Rubiaceae family, the same family as cleavers. Its aerial parts are used mainly as a flavoring, best known in German May wine (Maibowle), and in syrups, soft drinks and desserts. Its sweet, hay-like scent comes from coumarin, which forms from bound precursors called melilotosides as the cut herb wilts and dries. The herb also contains iridoids, chlorogenic acids and flavonoids. Folk medicine used it for digestion, coughs and unease, but no human trial has tested any health effect of woodruff; the research is lab and animal work. Coumarin is the main safety issue: in a small share of people it can harm the liver, so EU and German food-safety bodies set a tolerable intake for it. In the US, sweet woodruff is allowed as a natural flavoring in alcoholic beverages only.

Studied Dose No human dose of sweet woodruff has been tested. Safety limits apply to its coumarin instead: a tolerable daily intake of 0.1 mg per kg body weight (about 6 mg a day for a 60 kg adult). The coumarin content of woodruff varies with harvest and drying.
Active Compound Coumarin (formed from cis- and trans-melilotoside on drying), plus iridoid glycosides (monotropein, asperuloside, asperulosidic acid), chlorogenic acids and quercetin and kaempferol glycosides.

Benefits

Traditional flavoring herb for May wine, syrups and desserts

Sweet woodruff has a long history in Central and Northern Europe as an aromatic plant, steeped in white wine for May wine (Maibowle) and used in syrups, soft drinks, desserts and herbal preparations. Today its main role is flavor and scent. A recent review found no convincing clinical evidence for any defined woodruff preparation.

Hay-like aroma that develops as the cut herb wilts and dries

Fresh woodruff holds most of its coumarin in bound forms (melilotosides); in one analysis 88% of the coumarin in woodruff was released from these sugar-bound precursors. Wilting and drying free the coumarin and the scent. Lab work also found that long drying lowers coumarin again as it evaporates from the dried herb.

Folk uses for digestion, coughs and unease, not tested in people

In European folk medicine the herb was taken by mouth for digestive complaints, coughs and anxiety, and applied to wounds. No human study of any of these uses was found, so they rest on tradition; a recent review of the plant also found no convincing clinical evidence.

Fewer pro-inflammatory immune cells in mouse cell tests (lab study)

In mouse bone marrow macrophages pushed toward a pro-inflammatory (M1) state, an ethanol extract of the Latvian woodruff line richest in phenolics at 250 and 500 micrograms per mL cut the M1 share from 23% to 16% and 13%. It did not shift cells toward the calming M2 type. These are cell findings, not effects in people.

Paw swelling in rats given an oral leaf extract (animal study)

In an older screening of Italian medicinal plants, summarized in a recent review, an ethanol extract of woodruff leaves given by mouth at 100 mg per kg reduced chemically induced paw swelling in rats by 25%. This is a single animal screening test and has not been followed up in people.

Bacterial adhesion features in lab tests of a leaf extract (in vitro)

In a lab study of six Polish folk herbs against a urinary strain of E. coli, woodruff extract was one of the weaker inhibitors of bacterial growth, yet at 5 mg per mL and above the bacteria lost a red blood cell clumping sign of adhesion fibers, and biofilm fell. Drinking woodruff has not been tested for any urinary outcome.

Mechanism of action

1

Coumarin released from melilotoside precursors

In the living plant, coumarin is stored mainly as cis- and trans-melilotoside. When cells are damaged by wilting, drying or crushing, glycosidase enzymes split off the sugar and the freed acid closes into coumarin. This is why the scent, and the coumarin dose, depend on harvest time, drying and preparation.

2

Coumarin metabolism in the human liver

Coumarin is well absorbed, and in most people the liver enzyme CYP2A6 turns most of it into harmless 7-hydroxycoumarin. A minor route through other CYP enzymes forms a reactive epoxide; this route is thought to drive the liver injury seen in a small subset of people, though CYP2A6 gene variants alone did not explain who was affected.

3

Iridoids and phenolics beyond coumarin

Woodruff also contains iridoid glycosides (monotropein, asperuloside, asperulosidic acid and others), chlorogenic and neochlorogenic acid, and quercetin and kaempferol glycosides such as rutin. These compounds are active in cell and animal studies, but how much a woodruff tea or wine supplies has not been linked to any effect in people.

4

Coumarin is not a blood thinner

Coumarin shares part of its name with the drug warfarin, sold as Coumadin, but they differ. Warfarin and dicumarol are vitamin K antagonist derivatives, while plain coumarin, the compound in woodruff, is described in a review of its toxicology as having no anticoagulant activity.

Clinical trials

1
Woodruff Extract and Mouse Macrophage Polarization (in vitro)
PubMed

Laboratory study of 70% ethanol extracts of wild, sun-grown and shade-grown woodruff from Latvia: chemical profiling, antioxidant tests and effects on mouse bone marrow-derived macrophages. One author works for a cultivation company that the paper says had no role in the study. (Razzivina et al. 2024, Antioxidants (Basel))

No human participants; macrophages cultured from mouse bone marrow, plus chemical assays.

Coumarin stayed fairly stable across growing conditions, while sun-grown plants had more phenolics (mainly chlorogenic acid and rutin) and stronger antioxidant activity. At 250 and 500 micrograms per mL the extract lowered the share of pro-inflammatory M1 macrophages from 23% to 16% and 13%, without raising M2 cells, and was not toxic to the cells up to 750 micrograms per mL.

2
Six Folk Herbs and Urinary E. coli Virulence Traits (in vitro)
PubMed

Laboratory study of leaf extracts of birch, horsetail, rupturewort, sweet woodruff, nettle and lingonberry against a uropathogenic E. coli strain: growth, surface hydrophobicity, motility, adhesion fibers and biofilm. (Wojnicz et al. 2012, Urol Res)

No human participants; bacterial cultures.

Woodruff extract was among the weakest growth inhibitors of the six, though at 20 mg per mL bacterial survival fell to 37% of control. At 5 mg per mL and above the bacteria lost their red blood cell clumping ability, and like all six extracts it reduced biofilm, but it also increased swimming motility. Lab concentrations do not show any effect of drinking the herb.

3
Coumarin and Its Precursors During Post-Harvest Drying (lab analysis)
PubMed

Laboratory analysis of harvested woodruff shoots, measuring coumarin, cis-melilotoside and trans-melilotoside by UHPLC-DAD over 72 hours of drying, to examine the traditional pre-drying step for Maibowle. (Herre et al. 2025, Phytochemistry)

Harvested Galium odoratum plant material; no human or animal participants.

Drying was complete after 48 hours. trans-Melilotoside appeared to convert gradually to cis-melilotoside, and coumarin fell during longer drying because it sublimated, which the authors say supports using fresh or briefly air-dried herb with set drying times. Iridoids, chlorogenic acids and two flavonoid glycosides were also isolated. No intake or safety outcome was measured.

Side effects and drug interactions

Common Potential side effects

No human safety study of sweet woodruff itself was found; its risk is judged from its coumarin content.
Liver: as a drug at 90 to 400 mg a day, coumarin raised liver enzymes in a small subset of people (6% in one trial), usually reversibly; severe cases were rare. Food limits sit far lower, and the coumarin in a homemade tea or wine is not standardized.
Germany's BfR says the tolerable daily intake of 0.1 mg coumarin per kg (6 mg a day at 60 kg) also covers sensitive people, and that a slight excess for 1 to 2 weeks is not a health risk. Regular, heavy use is the concern.
Coumarin in a plant food was absorbed almost as well as pure coumarin in volunteers, so a woodruff preparation should not be assumed to be gentler than the isolated compound.
No safety data were found for pregnancy, breastfeeding or children; avoid concentrated woodruff products at those times.
May wine and other traditional woodruff drinks contain alcohol.

Important Drug interactions

No drug interaction studies of sweet woodruff were found.
Blood thinners such as warfarin: plain coumarin is described as having no anticoagulant activity, unlike warfarin and dicumarol, but woodruff has not been tested with these drugs; ask your prescriber.
Medicines that can affect the liver, and regular alcohol: coumarin can injure the liver in sensitive people, so combining them is a reasonable caution, though it has not been studied.
Coumarin is cleared mainly by the liver enzyme CYP2A6; whether drugs that change this enzyme alter coumarin risk has not been tested.

Frequently asked questions about Sweet Woodruff (Galium odoratum)

Is homemade May wine with woodruff a coumarin concern?

Germany's BfR says that a slight excess over the tolerable daily coumarin intake for one to two weeks is not a health risk, and that regular, heavy intake is what matters. No source we read measured coumarin in May wine. Coumarin forms as the herb wilts and long drying lowers it again, so the amount in a homemade batch is not predictable.

Can sweet woodruff be sold as a food flavoring in the US?

Only in a narrow way. FDA rules list sweet woodruff (Asperula odorata) as a natural flavoring for use in alcoholic beverages only. A separate rule treats food with added coumarin, as such or from tonka beans, as adulterated; that section does not name woodruff. The EU likewise bans adding coumarin as such and caps coumarin from flavoring ingredients in some foods.

Does the coumarin in woodruff thin the blood like warfarin?

No evidence says it does. Warfarin (Coumadin) and dicumarol are vitamin K antagonist derivatives, while plain coumarin, the compound in woodruff, is described in a toxicology review as having no anticoagulant activity. Woodruff has not been tested alongside blood thinners, so tell your prescriber if you use it often.

Why does woodruff smell stronger after it wilts?

Fresh woodruff stores its coumarin bound to sugar as melilotosides; in one analysis 88% of its coumarin came from these bound forms. Wilting, drying or crushing breaks the plant cells, enzymes release the coumarin, and the hay-like scent appears. Lab work found that very long drying lowers coumarin again as it evaporates.

Is sweet woodruff related to cleavers?

Yes. Both are in the genus Galium of the Rubiaceae family: sweet woodruff is Galium odoratum and cleavers is Galium aparine. Both contain iridoid glycosides, and woodruff is valued mainly for its coumarin aroma. See our cleavers page for that herb.

What is Sweet Woodruff?

Sweet woodruff (Galium odoratum, also listed as Asperula odorata) is a low woodland herb of the Rubiaceae family, the same family as cleavers. Its aerial parts are used mainly as a flavoring, best known in German May wine (Maibowle), and in syrups, soft drinks and desserts.

What is Sweet Woodruff used for?

NutraSmarts does not list Sweet Woodruff under a health category. What the research covers: Sweet woodruff has a long history in Central and Northern Europe as an aromatic plant, steeped in white wine for May wine (Maibowle) and used in syrups, soft drinks, desserts and herbal preparations. Today its main role is flavor and scent.

What is the recommended dosage of Sweet Woodruff?

No human dose of sweet woodruff has been tested. Safety limits apply to its coumarin instead: a tolerable daily intake of 0.1 mg per kg body weight (about 6 mg a day for a 60 kg adult). The coumarin content of woodruff varies with harvest and drying. Always follow the product label and check with a healthcare provider for personal advice.

Is Sweet Woodruff safe, and does it have side effects?

Side effects and cautions reported for Sweet Woodruff include: No human safety study of sweet woodruff itself was found; its risk is judged from its coumarin content. Liver: as a drug at 90 to 400 mg a day, coumarin raised liver enzymes in a small subset of people (6% in one trial), usually reversibly; severe cases were rare. It may also interact with some medications. Sweet Woodruff is not right for everyone, so check with a healthcare provider first if you are pregnant or breastfeeding, have a medical condition, or take prescription medication.

Does Sweet Woodruff interact with any medications?

Possible interactions include: No drug interaction studies of sweet woodruff were found. Blood thinners such as warfarin: plain coumarin is described as having no anticoagulant activity, unlike warfarin and dicumarol, but woodruff has not been tested with these drugs; ask your prescriber. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for Sweet Woodruff?

NutraSmarts rates the evidence for Sweet Woodruff as Preliminary (1 out of 5). It is backed by 3 study summaries and 15 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(15 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Herre I, Stegemann T. Sweet Woodruff (Galium odoratum L.)-More than Just Coumarin: From Fundamental to Biomass Valorization. Molecules. 2026;31(16):2920. doi: 10.3390/molecules31162920.PubMedUsed to support: Narrative review of sweet woodruff: traditional use in Maiwein and Maibowle, syrups, desserts and teas; folk use internally for digestive disorders, coughs and anxiety and externally for wounds; constituents (coumarin from cis- and trans-melilotoside, iridoids such as monotropein and asperuloside, chlorogenic acids, quercetin and kaempferol glycosides); an older rat screening in which an oral leaf extract (100 mg/kg) cut carrageenin paw edema by 25%; distinguishes coumarin from anticoagulant 4-hydroxycoumarin derivatives; cites the EFSA TDI of 0.1 mg/kg and EU Regulation 1334/2008. Concludes no convincing clinical evidence exists for defined woodruff preparations.
  2. Herre I, Stegemann T, Zidorn C. Comprehensive analysis of natural products of Galium odoratum (Rubiaceae), focusing on the formation of coumarin during the drying process. Phytochemistry. 2025;236:114485. doi: 10.1016/j.phytochem.2025.114485.PubMedUsed to support: Lab analysis of woodruff over 72 hours after harvest: drying was finished at 48 hours, trans-melilotoside appeared to isomerize to cis-melilotoside, and coumarin decreased during prolonged drying by sublimation, supporting fresh or briefly air-dried herb in Maibowle recipes. Iridoids, caffeoylquinic acids, flavonoid glycosides and the melilotosides were isolated. No human or animal participants.
  3. Rychlik M. Quantification of free coumarin and its liberation from glucosylated precursors by stable isotope dilution assays based on liquid chromatography-tandem mass spectrometric detection. J Agric Food Chem. 2008;56(3):796-801. doi: 10.1021/jf0728348.PubMedUsed to support: Analytical method study: coumarin was quantified in foods and plants, high in cassia products and lower in Ceylon cinnamon; in woodruff 88% of the total coumarin content was liberated from glucosylated precursors (68% in fenugreek seeds), whereas in cinnamon it was mainly free.
  4. Razzivina V, Vasiljeva A, Kronberga A, Skudrins G, Nakurte I, Zogota M, Mezaka I, Pugovics O, Grinberga S, Dambrova M, Sile I. Phenolic Content and Anti-Inflammatory Activity of Cultivated and Wild-Type Galium odoratum Extracts in Murine Bone Marrow-Derived Macrophages. Antioxidants (Basel). 2024;13(12):1447. doi: 10.3390/antiox13121447.PubMedUsed to support: Lab study: coumarin levels in woodruff extracts were stable across growing conditions, while sun-grown plants had more phenolics (chlorogenic acid, rutin) and antioxidant activity; extract at 250 and 500 µg/mL reduced LPS/IFN-γ-induced M1 mouse macrophages from 23% to 16% and 13% without increasing M2 cells, and was not toxic to the cells up to 750 µg/mL. No human participants.
  5. Wojnicz D, Kucharska AZ, Sokół-Łętowska A, Kicia M, Tichaczek-Goska D. Medicinal plants extracts affect virulence factors expression and biofilm formation by the uropathogenic Escherichia coli. Urol Res. 2012;40(6):683-97. doi: 10.1007/s00240-012-0499-6.PubMedUsed to support: Lab study of six herb extracts against uropathogenic E. coli: woodruff extract was among the weakest growth inhibitors (survival 37% of control at 20 mg/mL, where nettle was weaker), abolished hemagglutination (P fimbriae) at 5 mg/mL and above, increased swimming motility, and like all extracts reduced biofilm formation. Bacterial cultures only.
  6. Friesgaard KD, Fuglsang M, Aaboe ML, Rasmussen MB. [Christmas article: Can gin with herbs induce the vision of Christmas elves?]. Ugeskr Laeger. 2022;184(50):V80103..PubMedUsed to support: Humorous Christmas-issue randomized three-arm study (in Danish, English abstract) in 21 anesthesia registrars drinking gin with St. John's wort, angelica or sweet woodruff: seeing elves was not associated with sweet woodruff (p = 0.83), and the herbs did not relieve the medieval symptoms tested. No health outcome relevant to woodruff use; alcohol given to all.
  7. Abraham K, Wöhrlin F, Lindtner O, Heinemeyer G, Lampen A. Toxicology and risk assessment of coumarin: focus on human data. Mol Nutr Food Res. 2010;54(2):228-39. doi: 10.1002/mnfr.200900281.PubMedUsed to support: Review by German Federal Institute for Risk Assessment (BfR) scientists: coumarin is hepatotoxic; EFSA derived a TDI of 0.1 mg/kg body weight in 2004 from animal liver data, and human data from patients given coumarin as a drug, which revealed a more susceptible subgroup, gave the same TDI. Heavy consumers of cassia cinnamon may reach the TDI.
  8. Abraham K, Pfister M, Wöhrlin F, Lampen A. Relative bioavailability of coumarin from cinnamon and cinnamon-containing foods compared to isolated coumarin: a four-way crossover study in human volunteers. Mol Nutr Food Res. 2011;55(4):644-53. doi: 10.1002/mnfr.201000394.PubMedUsed to support: Crossover study in 24 healthy volunteers given 12 mg coumarin in four forms: relative absorption was 62.8% (isolated capsule), 56.0% (cinnamon capsules), 66.1% (cinnamon tea) and 54.7% (rice pudding); tea gave the fastest absorption and highest peaks. Coumarin in a plant matrix is absorbed only slightly less than isolated coumarin, so the TDI applies to food sources.
  9. Pitaro M, Croce N, Gallo V, Arienzo A, Salvatore G, Antonini G. Coumarin-Induced Hepatotoxicity: A Narrative Review. Molecules. 2022;27(24):9063. doi: 10.3390/molecules27249063.PubMedUsed to support: Review: coumarin, unlike dicumarol and warfarin (vitamin K antagonists), is devoid of anticoagulant activity; it is mainly metabolized by liver CYP2A6 to 7-hydroxycoumarin, while a minor epoxide pathway is thought to drive toxicity; hepatotoxicity, mostly mild to moderate and reversible transaminase rises, is limited to a small subset of patients, and CYP2A6*2 and *3 variants did not explain it. Describes EFSA's TDI of 0 to 0.1 mg/kg derived from a dog NOAEL of 10 mg/kg.
  10. Loprinzi CL, Kugler JW, Sloan JA, Rooke TW, Quella SK, Novotny P, Mowat RB, Michalak JC, Stella PJ, Levitt R, Tschetter LK, Windschitl H. Lack of effect of coumarin in women with lymphedema after treatment for breast cancer. N Engl J Med. 1999;340(5):346-50. doi: 10.1056/NEJM199902043400503.PubMedUsed to support: Randomized placebo-controlled crossover trial in 140 women: oral coumarin 200 mg twice daily for 6 months did not reduce arm volume (rise of 58 ml vs 21 ml on placebo, P = 0.80) or improve symptoms, and caused serologic evidence of liver toxicity in 6% of the women.
  11. Andréjak M, Gersberg M, Sgro C, Decocq G, Hamel JD, Morin M, Gras V. French pharmacovigilance survey evaluating the hepatic toxicity of coumarin. Pharmacoepidemiol Drug Saf. 1998;7 Suppl 1:S45-50. doi: 10.1002/(sici)1099-1557(199808)7:1+<s45::aid-pds353>3.3.co;2-t.PubMedUsed to support: French national survey of 34 liver reactions to synthetic coumarin used as a drug (average dose about 90 mg/day): causality likely or probable in 15, two positive rechallenges, mostly cytolytic, ALT above 10 times normal in 68%, 41% hospitalized; one liver transplant and two probable deaths, otherwise favorable outcomes. No risk factors identified.
  12. U.S. Food and Drug Administration (eCFR, accessed 2026). 21 CFR 172.510 Natural flavoring substances and natural substances used in conjunction with flavors. Electronic Code of Federal Regulations. 2026;Title 21, Part 172, Section 172.510; current text accessed October 2026..SourceUsed to support: Not PubMed-indexed. US food additive regulation listing natural flavoring substances that may be safely used in food in the minimum quantity required; the table lists "Woodruff, sweet" (Asperula odorata L.) with the limitation "In alcoholic beverages only".
  13. U.S. Food and Drug Administration (eCFR, accessed 2026). 21 CFR 189.130 Coumarin. Electronic Code of Federal Regulations. 2026;Title 21, Part 189, Section 189.130; 42 FR 14659, Mar. 15, 1977, as amended; accessed October 2026..SourceUsed to support: Not PubMed-indexed. Lists coumarin (1,2-benzopyrone) among substances prohibited from use in human food: food containing any added coumarin as such or as a constituent of tonka beans or tonka extract is deemed adulterated, based on a 1954 order. The section does not name woodruff.
  14. European Parliament and Council of the European Union. Regulation (EC) No 1334/2008 of 16 December 2008 on flavourings and certain food ingredients with flavouring properties for use in and on foods, Annex III. Official Journal of the European Union. 2008;OJ L 354, 31.12.2008; text as adopted, read via legislation.gov.uk, accessed October 2026..SourceUsed to support: Not PubMed-indexed. Annex III Part A lists 1,2-benzopyrone (coumarin) among substances not to be added as such to food; Part B sets maximum coumarin levels in compound foods as consumed when it comes from flavorings or food ingredients with flavoring properties: 50 mg/kg in traditional or seasonal bakery ware labeled with cinnamon, 20 mg/kg in breakfast cereals including muesli, 15 mg/kg in other fine bakery ware and 5 mg/kg in desserts.
  15. German Federal Institute for Risk Assessment (BfR). Frequently asked questions on coumarin in cinnamon and other foods. Bundesinstitut für Risikobewertung (BfR). 2012;FAQ dated 27 September 2012; accessed October 2026..SourceUsed to support: Not PubMed-indexed. German risk assessment FAQ: coumarin occurs in woodruff, tonka beans and melilot; the TDI is 0.1 mg per kg body weight per day and also applies to especially sensitive consumers (6 mg a day for a 60 kg adult); short-term or slight exceedance for one to two weeks is not considered a health risk; liver effects seen in sensitive people taking coumarin as a drug are usually reversible. No coumarin level for woodruff is given.