slippery elm
Slippery Elm (Ulmus Rubra) is a dietary supplement.
Ulmus Rubra
Key facts
- Active ingredient
- Ulmus Rubra
- Type
- Supplement
What is Slippery Elm?
From the FDA label:An herbal mucilage traditionally used to soothe the digestive tract and throat.
What the evidence says
Limited evidenceWhat Slippery Elm is
Commonly used for
What the evidence shows
Typical dosage
Safety
Side effects
Interactions & cautions
This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. Summarized from public health authorities; general reference, not medical advice. Talk to a licensed healthcare professional before starting any supplement.
Ways to save
Ask for the generic
Same active ingredient, far cheaper. Is there a generic? →
Request a 90-day supply
Bulk fills usually lower the per-dose price vs monthly refills.
Use copay cards
Manufacturer copay cards & patient-assistance programs — especially for brand drugs.
Compare alternatives
A same-class option may cost less. See alternatives →
Information is sourced from public FDA regulatory data. Provided for general reference only — not medical advice. Always consult a licensed professional and the current prescribing information.
What people report to the FDA about Ulmus Rubra
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 16 reports naming Ulmus Rubra — the active ingredient in Slippery Elm, and the FDA flagged 94% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:
- aphasia9 reports
- dysarthria9 reports
- gastrointestinal disorder9 reports
- hypoaesthesia oral9 reports
- mastication disorder9 reports
- paraesthesia9 reports
- pollakiuria9 reports
- chronic kidney disease2 reports
Read these as a signal, not a rate. A report does not mean Ulmus Rubra caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label.
Source: openFDA drug/event (FAERS), retrieved September 26, 2026.
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