boswellia
Boswellia (Boswellia Serrata) is a dietary supplement.
Boswellia Serrata
Key facts
- Active ingredient
- Boswellia Serrata
- Type
- Supplement
What is Boswellia?
From the FDA label:An herbal resin (frankincense) traditionally used for joint comfort.
What the evidence says
What Boswellia 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.
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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 Boswellia Serrata
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 182 reports naming Boswellia Serrata — the active ingredient in Boswellia, and the FDA flagged 53% 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:
- fatigue25 reports
- arthralgia14 reports
- constipation11 reports
- peripheral swelling11 reports
- diarrhoea10 reports
- dyspnoea10 reports
- nausea10 reports
- pruritus10 reports
Read these as a signal, not a rate. A report does not mean Boswellia Serrata 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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