Iceland Moss (Cetraria islandica)

Cetraria islandica
Evidence Level
Preliminary
6 Clinical Trials
6 Documented Benefits
1/5 Evidence Score

Iceland moss is not a true moss but a lichen of northern and mountain regions, used for centuries in European herbal medicine. Its dried thallus is 25 to 50 percent polysaccharides, mainly lichenan and isolichenan, which swell in water into a soothing mucilage, plus bitter lichen acids. It is sold as lozenges, teas and tinctures. The European Medicines Agency accepts it only as a traditional herbal medicine, based on long-standing use: as a demulcent for an irritated mouth or throat with an associated dry cough, and for temporary loss of appetite. The agency found no placebo-controlled trials. The human data are a small randomized comparison of three lozenge strengths after nasal surgery, with no placebo group, and a large uncontrolled survey of lozenge tolerability in children. Wild lichen can concentrate lead and other metals from the air, so pharmacopoeia-grade material matters.

Studied Dose Lozenges equal to 0.48, 3 or 5 g of dried lichen a day for 5 days were compared (strengths per the EMA report), with no difference between strengths; children took mostly 4 to 6 lozenges a day (80 or 100 mg extract each). EU traditional tea: 4 to 6 g of dried lichen a day.
Active Compound Mucilage polysaccharides (25 to 50 percent of the dried lichen), mainly lichenan (a beta-glucan) and isolichenan (an alpha-glucan); bitter lichen acids, chiefly fumarprotocetraric and protolichesterinic acid.

Benefits

Soothing film for the mouth and throat in EU traditional use

Iceland moss is registered in the EU as a traditional herbal medicine used as a demulcent for an irritated mouth or throat and the dry cough that can come with it. That status rests on at least 30 years of documented use. The regulator found no placebo-controlled trials, and the clinical reports it reviewed were small and had no placebo group.

Mouth and throat dryness after nasal surgery in a lozenge dose study

In 61 adults breathing only through the mouth after nasal surgery, lozenges equal to 0.48, 3 or 5 g of dried lichen a day (strengths as given by EU regulators) were compared for 5 days. Dryness, coating and inflammation improved in all three groups with no difference between doses. There was no placebo group, so natural recovery after surgery cannot be ruled out.

Lozenge tolerability in children aged 4 to 12

In a post-marketing survey of 3,143 children with upper airway complaints who sucked Iceland moss lozenges for 1 to 2 weeks, possible reactions occurred in 6 children (0.2 percent): itching, nausea, stomach upset or mouth burning, all passing on their own. Most children were rated recovered or improved by the end, but with no control group this cannot be credited to the lozenges.

Traditional bitter used to support appetite

EU regulators also accept Iceland moss tea for temporary loss of appetite in adults, based on its use as a bitter. They found no clinical or laboratory studies of this use and judged it plausible only because the lichen acids taste bitter. Persistent loss of appetite needs a medical check.

Lichenan gel that resembles a saliva mucin in lab tests

In a laboratory comparison of plant gels as possible saliva substitutes, lichenan from Iceland moss came closest to the main salivary mucin and, once buffered, clung to human cheek cells about as firmly as natural saliva. In an older pig cheek tissue test, as summarized by EU regulators, its polysaccharides adhered only slightly. Neither was a study in people.

Immune cell signaling in cell and rat studies

In human immune cells grown in a dish, a water extract raised both IL-10, an anti-inflammatory messenger, and IL-12, with IL-10 rising more, an effect traced to lichenan. Injected under the skin of rats, the extract reduced induced arthritis, at the highest of three doses only according to an EU review. Neither result shows an effect from swallowing Iceland moss.

Mechanism of action

1

Swelling polysaccharides coat the mouth and throat

Lichenan, a hot water soluble beta-glucan, and isolichenan, a cold water soluble alpha-glucan, make up much of the dried lichen and swell into a viscous mucilage. Sucked slowly as a lozenge or sipped as tea, it is thought to form a protective film on the lining of the mouth and throat. How long that film lasts has not been measured in people.

2

Bitter lichen acids behind the appetite tradition

Fumarprotocetraric acid (about 2.6 to 11.5 percent) and protolichesterinic acid (about 0.1 to 1.5 percent) give the lichen its bitterness, the basis for its use as a bitter. They dissolve poorly in cold water. In a simulated digestion model, protolichesterinic and related paraconic acids stayed stable, and they acted as antioxidants in intestinal cells in a dish.

3

Lichenan shifts immune cell messengers in vitro

In human dendritic cells, lichenan reproduced the extract's rise in IL-10 relative to IL-12, while isolichenan and the lichen acids were inactive. This is a cell culture effect at set concentrations; whether any lichenan reaches immune tissue after swallowing is unknown.

Clinical trials

1
Three Strengths of Iceland Moss Lozenges After Nasal Surgery (no placebo)
PubMed

Randomized comparison of three concentrations of Iceland moss extract lozenges (Isla-Moos), given from the first to the fifth day after nasal septum surgery; the EMA review describes it as double-blind with no placebo arm. Article in German with an English abstract. (Kempe et al. 1997, Laryngorhinootologie)

61 patients (63 in the EMA summary, aged 18 to 65) breathing through the mouth because of nasal packing after surgery on the nasal septum.

Mucosal coating, dryness and inflammation, tongue coating, hoarseness and sore throat improved in all groups, with no significant difference between lozenges equal to 0.48, 3 or 5 g of dried lichen a day (strengths from the EMA summary; the abstract states only the 0.48 g dose). The authors concluded the lowest dose (10 lozenges a day) was enough. With no placebo, the improvement cannot be separated from normal healing after surgery. No side effects were reported.

2
Iceland Moss Lozenges in 3,143 Children: Post-Marketing Tolerability Survey (uncontrolled)
PubMed

Multicenter post-marketing surveillance study in about 300 mainly pediatric practices in Germany of Isla-Moos (80 mg aqueous extract) and Isla-Mint (100 mg) lozenges; the first author's listed affiliation is the German drug company Engelhard Arzneimittel. Article in German with an English abstract. (Hecker et al. 2004, Forsch Komplementarmed Klass Naturheilkd)

3,143 children aged 4 to 12 with upper respiratory complaints (1,848 Isla-Moos, 1,295 Isla-Mint), treated for 1 to 2 weeks; 61 percent took 4 to 6 lozenges a day.

73 adverse events in 57 children (1.8 percent) were mostly attributed to the underlying illness. Seven events in 6 children (0.2 percent) were possibly related: itching twice, nausea twice, abdominal pain, heartburn and mouth burning, all resolving on their own. By the end, 39 percent were rated fully recovered and 55 percent improved, but with no control group these symptom figures do not show efficacy.

3
Iceland Moss Extract and Lichenan on Immune Cells and Rat Arthritis (lab and animal)
PubMed

Laboratory study of a traditionally prepared water extract and purified compounds (lichenan, isolichenan, protolichesterinic and fumarprotocetraric acids), plus a rat model of induced arthritis. No human participants. (Freysdottir et al. 2008, Int Immunopharmacol)

Human monocyte-derived dendritic cells in culture, and rats with antigen-induced arthritis given the extract by injection under the skin.

The extract raised secretion of both IL-10 and IL-12p40, with IL-10 more prominent; lichenan did the same, while isolichenan and the lichen acids were inactive. Rats given the extract developed significantly less arthritis than saline-treated rats (according to the EMA summary, only at the highest of three doses). The extract was injected, not swallowed.

4
Lichenan as a Saliva Mucin Mimic: Laboratory Comparison of Plant Gels
PubMed

Laboratory study comparing water extracts of calendula, Fucus seaweed and lichenan from Iceland moss as candidate saliva substitutes, including a new adhesion test with human buccal cells. No human participants. (Winter et al. 2024, Pharmaceutics)

Plant polysaccharide preparations tested against human saliva and human buccal epithelial cells.

Lichenan was the best candidate to mimic the salivary mucin MUC5B. After its pH, osmolality and buffering were adjusted, it showed high cell adhesion, with a maximum detachment force comparable to unstimulated whole mouth saliva. This supports the idea of a mucilage film but does not show relief of dry mouth in people.

5
Iceland Moss as a Famine Food: Mouse and Rat Feeding Tests (animal)
PubMed

Animal feeding study of traditional emergency foods in Finland, including Iceland moss given untreated or after the traditional wood ash soaking and boiling. No human participants. (Airaksinen et al. 1986, J Ethnopharmacol)

Mice fed diets of 50 percent plant material, and rats fed 25 percent ash-treated Iceland moss for 3 months.

No 50 percent mixture was tolerated by mice. Rats tolerated 25 percent ash-treated lichen rather well but gained less weight, and at the end had protein in the urine and kidney tubule changes, which the authors linked to high lead levels in the lichen and in the rats' kidneys. These are food-scale amounts, far above supplement doses.

6
Trace Metals in 14 Market Samples of Iceland Moss and Their Teas (lab analysis)
PubMed

Laboratory analysis of 14 samples of cut, dried Iceland moss bought from different suppliers on the European market, measuring trace elements in the raw lichen and in the decoction made from it. No human participants. (Giordani et al. 2017, Chemosphere)

14 commercial samples of dried Iceland moss and their decoctions.

Arsenic, cadmium, lead, nickel and other elements were measured. Levels in the decoctions were significantly lower than in the raw lichen, down to levels of negligible health concern, and differences between suppliers seen in the raw material disappeared in the teas. Transfer from lichen to tea ranged from 2 percent for copper to 95 percent for zinc.

Side effects and drug interactions

Common Potential side effects

In 3,143 children using Iceland moss lozenges, possible reactions occurred in 0.2 percent: itching, nausea, abdominal pain, heartburn and burning in the mouth, all passing on their own.
The EU monograph lists no known side effects. A 2021 EU review of 92 European adverse event reports mentioning Iceland moss found only 4 linked specifically to it (allergic reaction, vomiting, cough, diarrhea) and could not establish that it caused them.
Do not use if you are allergic to Iceland moss. Patch tests in people with light-sensitive dermatitis found contact allergy to lichen mixtures, including Iceland moss.
Wild lichen absorbs metals from the air: according to the EU assessment report, samples from southern Finland held about 30 mg/kg of lead, and the European Pharmacopoeia limits lead in medicinal Iceland moss to 10 ppm, so choose products made to that standard.
Raw lichen eaten as a large share of the diet was toxic to mice, and rats fed ash-treated lichen for 3 months showed kidney changes linked to its lead content. Do not eat untreated lichen as food.
Not recommended in pregnancy or breastfeeding, as safety has not been studied. EU guidance does not recommend the tea under age 12, lozenges under age 6, or tinctures under 18.
See a doctor if symptoms last more than a week, or if shortness of breath, fever or pus-like phlegm appears.

Important Drug interactions

No interaction studies exist, and the EU monograph reports no interactions; the points below are precautions.
Other oral medicines: the mucilage may delay their absorption, a possibility that has not been tested in people or animals. EU guidance advises taking Iceland moss half an hour to 1 hour apart from other medicines.
Tinctures are made with 40 percent ethanol, so the usual alcohol cautions apply, including with medicines that should not be combined with alcohol.

Frequently asked questions about Iceland Moss (Cetraria islandica)

Is Iceland moss actually a moss?

No. Despite the name it is a lichen, a member of the Parmeliaceae family, that grows in arctic and subarctic regions and in mountain areas of Europe, Siberia and North America. The medicinal part is the dried, branching thallus, which is greenish brown on top and pale underneath. Pharmacopoeia-grade material must swell in water to a set minimum, a sign of its mucilage content.

Why are Iceland moss lozenges meant to dissolve slowly in the mouth?

The traditional use is local: the swelling polysaccharides are meant to coat an irritated mouth and throat on contact, so the lozenge is dissolved slowly in the mouth and swallowed rather than chewed or swallowed whole; EU guidance lists these lozenge extracts for use in the mouth. The human studies used lozenges sucked several times a day. How long any coating lasts has not been measured in people.

Does the lichen pick up lead or other metals from the air?

Yes. Lichens lack a protective outer layer and absorb airborne metals; samples from southern Finland held about 30 mg/kg of lead according to the EU assessment report, and Italian herbarium samples tracked the fall in lead after leaded fuel was banned. The same report notes that the European Pharmacopoeia caps lead in medicinal Iceland moss at 10 ppm, and tests of 14 market samples found far lower metal levels in the tea than in the raw lichen.

Can Iceland moss be eaten as a food?

It was once eaten in northern Europe as famine food and in bread or dessert jelly, after soaking in wood ash and boiling to remove the bitter acids. In a Finnish feeding study, as summarized by EU regulators, untreated lichen as half of the diet killed mice within 4 to 5 days, and rats fed treated lichen for 3 months showed kidney changes linked to lead. Supplement doses are far smaller than food amounts.

What is Iceland Moss?

Iceland moss is not a true moss but a lichen of northern and mountain regions, used for centuries in European herbal medicine. Its dried thallus is 25 to 50 percent polysaccharides, mainly lichenan and isolichenan, which swell in water into a soothing mucilage, plus bitter lichen acids.

What is Iceland Moss used for?

NutraSmarts does not list Iceland Moss under a health category. What the research covers: Iceland moss is registered in the EU as a traditional herbal medicine used as a demulcent for an irritated mouth or throat and the dry cough that can come with it. That status rests on at least 30 years of documented use.

What is the recommended dosage of Iceland Moss?

The clinically studied dose is Lozenges equal to 0.48, 3 or 5 g of dried lichen a day for 5 days were compared (strengths per the EMA report), with no difference between strengths; children took mostly 4 to 6 lozenges a day (80 or 100 mg extract each). Always follow the product label and check with a healthcare provider for personal advice.

Is Iceland Moss safe, and does it have side effects?

Side effects and cautions reported for Iceland Moss include: In 3,143 children using Iceland moss lozenges, possible reactions occurred in 0.2 percent: itching, nausea, abdominal pain, heartburn and burning in the mouth, all passing on their own. The EU monograph lists no known side effects. It may also interact with some medications. Iceland Moss 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 Iceland Moss interact with any medications?

Possible interactions include: No interaction studies exist, and the EU monograph reports no interactions; the points below are precautions. Other oral medicines: the mucilage may delay their absorption, a possibility that has not been tested in people or animals. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for Iceland Moss?

NutraSmarts rates the evidence for Iceland Moss as Preliminary (1 out of 5). It is backed by 6 study summaries and 14 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(14 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. European Medicines Agency, Committee on Herbal Medicinal Products (HMPC). European Union herbal monograph on Cetraria islandica (L.) Acharius s.l., thallus. Final. European Medicines Agency. 2015;EMA/HMPC/678891/2013. Adopted 24 November 2014; published 11 February 2015..SourceUsed to support: Not PubMed-indexed; official EU regulatory document. Accepts Iceland moss only as a traditional herbal medicine: as a demulcent for oral or throat irritation with associated dry cough, and for temporary loss of appetite. Gives the tea, lozenge extract and tincture doses, the age limits, the one-week limit without medical advice, the advice to separate it from other medicines by half an hour to 1 hour, no known side effects, and no data in pregnancy.
  2. European Medicines Agency, Committee on Herbal Medicinal Products (HMPC). Assessment report on Cetraria islandica (L.) Acharius s.l., thallus. Final. European Medicines Agency. 2015;EMA/HMPC/36866/2014. Adopted 24 November 2014; published 11 February 2015..SourceUsed to support: Not PubMed-indexed; official EU regulatory review. Lists constituents (25 to 50 percent polysaccharides including lichenan and isolichenan; fumarprotocetraric and protolichesterinic acids), lead of 30 mg/kg in Finnish samples and the 10 ppm pharmacopoeia lead limit, and patch test allergy data. Concludes there are no controlled clinical studies and summarizes the small lozenge studies, including an open 100-patient study of lozenges that also contained hogweed extract.
  3. European Medicines Agency, Committee on Herbal Medicinal Products (HMPC). Addendum to assessment report on Cetraria islandica (L.) Acharius s.l., thallus. European Medicines Agency. 2022;EMA/HMPC/502105/2021. Adopted 24 November 2021; published 8 March 2022..SourceUsed to support: Not PubMed-indexed; official EU periodic review. Found no new clinical efficacy or safety data published from 2013 to 2021. Of 92 EudraVigilance reports mentioning Iceland moss, 4 related specifically to it (hypersensitivity, vomiting, cough, diarrhea), and causality could not be established. The monograph was left unchanged.
  4. Kempe C, Grüning H, Stasche N, Hörmann K. [Icelandic moss lozenges in the prevention or treatment of oral mucosa irritation and dried out throat mucosa]. Laryngorhinootologie. 1997;76(3):186-8. doi: 10.1055/s-2007-997409.PubMedUsed to support: Randomized comparison of three Iceland moss lozenge strengths in 61 patients with mouth and throat dryness after nasal septum surgery, for 5 days. All groups improved with no significant difference between doses; 0.48 g of lichen a day (10 lozenges) was judged sufficient. No placebo group, so the improvement cannot be separated from normal recovery.
  5. Hecker M, Völp A. [Tolerability of Icelandic moss lozenges in upper respiratory tract diseases - multicentric drug monitoring study with 3,143 children]. Forsch Komplementarmed Klass Naturheilkd. 2004;11(2):76-82. doi: 10.1159/000078228.PubMedUsed to support: Uncontrolled post-marketing survey of 3,143 children aged 4 to 12 using Iceland moss lozenges for 1 to 2 weeks: possible adverse reactions in 6 children (0.2 percent), all mild and transient. Symptom ratings improved, but with no control group this is a tolerability record, not proof of efficacy. First author affiliated with Engelhard Arzneimittel.
  6. Airaksinen MM, Peura P, Ala-Fossi-Salokangas L, Antere S, Lukkarinen J, Saikkonen M, Stenbäck F. Toxicity of plant material used as emergency food during famines in Finland. J Ethnopharmacol. 1986;18(3):273-96. doi: 10.1016/0378-8741(86)90006-1.PubMedUsed to support: Animal feeding study: 50 percent mixtures of famine plants, including Iceland moss, were not tolerated by mice; rats fed 25 percent ash-treated Iceland moss for 3 months developed proteinuria and kidney tubule changes, probably from high lead in the lichen. Food-scale exposure, not supplement doses.
  7. Giordani P, Minganti V, Brignole D, Malaspina P, Cornara L, Drava G. Is there a risk of trace element contamination in herbal preparations? A test study on the lichen Cetraria islandica. Chemosphere. 2017;181:778-785. doi: 10.1016/j.chemosphere.2017.04.140.PubMedUsed to support: Analysis of 14 European market samples of dried Iceland moss: trace elements including lead and cadmium were much lower in decoctions than in the raw lichen, down to levels of negligible health concern, with transfer ranging from 2 percent (copper) to 95 percent (zinc).
  8. Minganti V, Drava G, De Pellegrini R, Modenesi P, Malaspina P, Giordani P. Temporal trends (1981-2007) of trace and rare earth elements in the lichen Cetraria islandica (L.) Ach. from Italian herbaria. Chemosphere. 2014;99:180-5. doi: 10.1016/j.chemosphere.2013.10.067.PubMedUsed to support: In 24 Italian herbarium specimens of Iceland moss collected from 1981 to 2007, lead fell over time in line with the ban on leaded fuel, and before 1995 was higher closer to a highway, showing that the lichen records airborne metal pollution.
  9. Freysdottir J, Omarsdottir S, Ingólfsdóttir K, Vikingsson A, Olafsdottir ES. In vitro and in vivo immunomodulating effects of traditionally prepared extract and purified compounds from Cetraria islandica. Int Immunopharmacol. 2008;8(3):423-30. doi: 10.1016/j.intimp.2007.11.007.PubMedUsed to support: A water extract raised IL-10 more than IL-12p40 in human dendritic cells in culture, an effect reproduced by lichenan but not isolichenan or the lichen acids; injected under the skin, the extract reduced induced arthritis in rats. Cell and animal work only.
  10. Winter C, Tetyczka C, Pham DT, Kolb D, Leitinger G, Schönfelder S, Kunert O, Gerlza T, Kungl A, Bucar F, Roblegg E. Investigation of Hydrocolloid Plant Polysaccharides as Potential Candidates to Mimic the Functions of MUC5B in Saliva. Pharmaceutics. 2024;16(5):682. doi: 10.3390/pharmaceutics16050682.PubMedUsed to support: Laboratory study: of calendula, Fucus and Iceland moss lichenan, lichenan best mimicked the salivary mucin MUC5B and, once buffered, adhered to human buccal cells with a detachment force comparable to unstimulated saliva. No human participants.
  11. Schmidgall J, Schnetz E, Hensel A. Evidence for bioadhesive effects of polysaccharides and polysaccharide-containing herbs in an ex vivo bioadhesion assay on buccal membranes. Planta Med. 2000;66(1):48-53. doi: 10.1055/s-2000-11118.PubMedUsed to support: Ex vivo test of plant polysaccharides on pig cheek membranes showing concentration-dependent adhesion of some mucilages to the tissue surface. According to the EMA assessment report, Iceland moss polysaccharides adhered only slightly (about 10 percent) in this assay.
  12. Krämer P, Wincierz U, Grübler G, Tschakert J, Voelter W, Mayer H. Rational approach to fractionation, isolation, and characterization of polysaccharides from the lichen Cetraria islandica. Arzneimittelforschung. 1995;45(6):726-31..PubMedUsed to support: Describes lichenan, isolichenan and a galactomannan as the polysaccharides of pharmaceutical interest, notes that isolichenan is used as an active ingredient in cough lozenges, and shows that extraction temperature and pH strongly change polysaccharide and tannin yields.
  13. Sánchez M, Ureña-Vacas I, González-Burgos E, Divakar PK, Gómez-Serranillos MP. The Genus Cetraria s. str.-A Review of Its Botany, Phytochemistry, Traditional Uses and Pharmacology. Molecules. 2022;27(15):4990. doi: 10.3390/molecules27154990.PubMedUsed to support: Review of the genus: Cetraria islandica is the most studied species, contains depsidones (fumarprotocetraric and protocetraric acids) and fatty acids (lichesterinic and protolichesterinic acids), and has been used in folk medicine for digestive and respiratory complaints as decoctions, tinctures, extracts and infusions. The pharmacology it reviews is laboratory and animal work.
  14. Villicaña González E, Sanchez Armengol E, Breynaert A, Lauwers S, Foubert K, Rispoli RM, Pieters L, Stuppner H, Marzocco S, Hermans N, Laffleur F, Schwaiger S. Insights in pharmacological activities and the gastrointestinal stability of paraconic acids from Cetraria islandica (L.) Ach. J Ethnopharmacol. 2026;370:122065. doi: 10.1016/j.jep.2026.122065.PubMedUsed to support: Laboratory study: paraconic acids such as protolichesterinic acid, which pass into hot water preparations, showed antioxidant and wound healing effects in stimulated intestinal epithelial cells and remained stable through a simulated digestion model including a colon phase. No human participants.