echinacea
Echinacea is a dietary supplement.
Generic
Key facts
- Active ingredient
- Echinacea
- Form
- Tablet, orally disintegrating
- Type
- Supplement
What is Echinacea?
From the FDA label:Dosage Adults take 1 tablet three times daily, dissolving on the tongue. For severe symptoms, take one tablet every hour until improvement is felt. Children receive 1/2 tablet as above.
What the evidence says
What Echinacea 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.
How to use
(Read Suggested Use Section)
Warnings
Important safety information
If pregnant or breast-feeding, consult a health professional before use.
Dosage forms
Tablet, orally disintegrating
The forms currently marketed in the U.S., per the FDA National Drug Code Directory.
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 →
Frequently asked questions
- What forms does Echinacea come in?
- Echinacea is currently marketed as tablet, orally disintegrating, per the FDA's National Drug Code Directory.
- Is Echinacea safe?
- There's no single safe-or-not verdict, and we don't yet have a composite recall-safety score for Echinacea. Review its FDA-label side effects and warnings below, and always consult a licensed professional.
Clinical content sourced from the FDA label via openFDA (U.S. FDA). View the FDA label on DailyMed → 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 Echinacea
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 1,854 reports naming Echinacea, and the FDA flagged 57% 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:
- fatigue182 reports
- nausea156 reports
- diarrhoea129 reports
- headache123 reports
- arthralgia110 reports
- dizziness105 reports
- dyspnoea96 reports
- asthenia83 reports
Read these as a signal, not a rate. A report does not mean Echinacea 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 25, 2026.
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