melatonin
Melatonin is a dietary supplement.
Generic
Key facts
- Active ingredient
- Melatonin
- Form
- Liquid
- Type
- Supplement
What the evidence says
What Melatonin 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.
Dosage forms
Liquid
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 Melatonin come in?
- Melatonin is currently marketed as liquid, per the FDA's National Drug Code Directory.
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 Melatonin
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 56,018 reports naming Melatonin, and the FDA flagged 66% 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:
- fatigue4,591 reports
- nausea3,907 reports
- diarrhoea3,136 reports
- headache3,099 reports
- dyspnoea2,690 reports
- insomnia2,617 reports
- fall2,499 reports
- dizziness2,452 reports
Read these as a signal, not a rate. A report does not mean Melatonin 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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