Benefits
Traditional herbal use as an expectorant for cough
In the EU, white horehound tea and extracts are registered as a traditional herbal medicine used as an expectorant for cough. The registration rests only on long-standing use, not on clinical trials. In the US, the FDA lists horehound among expectorant ingredients without adequate data to show safety and effectiveness for over-the-counter use.
Cough scores in a children's multi-herb syrup trial
In a small placebo-controlled trial in 56 children aged 5 to 11 with a recent cough, a syrup combining horehound flower extract with ivy, sundew, plantain and eucalyptus honey lowered day and night cough scores more than placebo over 7 days. Because horehound was one of five ingredients, the result cannot be credited to horehound alone. The trial was industry-sponsored.
Traditional bitter herb for digestive comfort and appetite
Its bitter taste, mainly from marrubiin, is the basis for traditional use before meals for occasional bloating, flatulence and temporary loss of appetite. The EU recognizes this use on the basis of long-standing use only, with the herb taken about half an hour before meals. No controlled human trials of these uses were found.
Blood sugar and blood lipids in one small human trial
In a 21-day randomized study, 21 adults with poorly controlled type 2 diabetes added a horehound leaf infusion to their usual treatment. Fasting glucose fell by only 0.64%, cholesterol by 4.16% and triglycerides by 5.78%, and the comparison herb did better. There was no placebo group, and the result does not support a blood sugar benefit.
Stomach lining and gut muscle effects in animal and lab studies
Animal and lab work only. In mice, a horehound leaf extract and marrubiin reduced stomach lining damage from alcohol or indomethacin and raised stomach pH and mucus. In isolated smooth muscle tissue, a hydroalcoholic extract relaxed contractions caused by several chemical messengers. These findings have not been tested in people.
Pain-signal effects of marrubiin in mouse studies
Animal work only. Marrubiin injected into mice reduced pain responses in several chemical pain tests in a dose-related way, but it did not change heat-pain response and its effect was not blocked by naloxone, which suggests it does not act through opioid pathways. Injected doses in mice do not show an effect from horehound tea in people.
Mechanism of action
Marrubiin, the main bitter compound
Marrubiin is a labdane diterpene that is characteristic of the Marrubium genus and the main source of the herb's bitterness, typically about 0.12 to 1% of the plant. Bitter compounds are thought to prompt digestive and bile secretions, which is the traditional rationale for taking the herb before meals.
Stomach-lining defense signals in mice
In mice, the protective effect of the extract and marrubiin on the stomach lining went along with higher stomach pH and more mucus, and was linked to nitric oxide and the lining's own sulfhydryl compounds. Separately, an extract relaxed smooth muscle contractions in isolated tissue, with apparent selectivity for acetylcholine-driven contractions.
Antioxidant phenolic compounds
Horehound contains phenylethanoid glycosides such as acteoside, plus flavonoids and phenolic acids. In test-tube work, a water extract slowed copper-driven oxidation of human LDL and increased HDL-driven cholesterol release from cultured macrophages. Whether drinking the tea has these effects in people is unknown.
Clinical trials
Pilot, randomized, double-blind, placebo-controlled, multicenter trial of Sediflù syrup (eucalyptus honey with dry extracts of horehound flowers, sundew, ivy leaf and plantain leaf), 10 ml twice daily for 7 days; sponsored by Cinfa Laboratories (Núñez et al. 2024, Clin Pediatr (Phila))
56 children aged 5 to 11 years with dry or productive cough lasting 3 to 7 days (27 on syrup, 29 on placebo); 60 were recruited.
Daytime cough scores were significantly lower than placebo from day 3 and nighttime scores from day 4 through day 7. No adverse effects were observed in either group. The amount of horehound per dose was not stated, horehound was one of four herbal extracts plus honey, coughs were milder than expected, and baseline scores were slightly higher in the syrup group.
Randomized, double-blind 21-day study comparing a Marrubium vulgare dry-leaf infusion with a Cecropia obtusifolia infusion, both added to usual treatment; no placebo group (Herrera-Arellano et al. 2004, Phytomedicine)
43 outpatients with poorly controlled type 2 diabetes; 21 received horehound and 22 received Cecropia.
In the horehound group fasting glucose fell by 0.64%, cholesterol by 4.16% and triglycerides by 5.78%. The between-group comparison found significant differences in glucose and cholesterol lowering, and the authors' positive conclusion concerned the Cecropia infusion, not horehound. A later review noted that this result contradicted earlier mouse studies.
Mouse study of a methanol leaf extract (25 to 100 mg/kg) and isolated marrubiin (25 mg/kg) in alcohol-induced and indomethacin-induced stomach injury models, with omeprazole or cimetidine as reference drugs (Paula de Oliveira et al. 2011, J Pharm Pharmacol)
Mice; no human participants.
In the indomethacin model, ulcer inhibition was about 50%, 66% and 82% at 25, 50 and 100 mg/kg of extract, versus about 68% for cimetidine. Marrubiin significantly reduced all measured injury parameters in both models. Extract and marrubiin raised stomach pH and mucus, with effects linked to nitric oxide and sulfhydryl compounds. Not tested in people.
Mouse study of marrubiin isolated from Marrubium vulgare, given by injection into the abdominal cavity, in writhing, formalin, capsaicin and hot-plate pain tests (De Jesus et al. 2000, Phytomedicine)
Mice; no human participants.
Marrubiin produced dose-related reductions in pain responses, with ID50 values of 2.2 (writhing), 6.6 and 6.3 (formalin first and second phase) and 28.8 micromol/kg (capsaicin). It did not lengthen hot-plate latency, and naloxone did not reverse its effect, so the authors suggest no opioid involvement. Injected doses in mice, not oral use in people.