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Legal status · United States

Is NDGA legal in the United States?

Written by Reviewed Sep 2026

Not approvedLongevityNo human studies cited

Direct answer

No. NDGA is not an approved medicine in the United States; its classification is "Not approved; research use only". Nothing containing it is authorized for any use in people. Vials labeled "for research use only" are not exempt: that label does not make human use lawful. On the evidence, no human study is cited on its profile.

NDGA in the United States at a glance

ClassificationNot approved; research use only
NoteNo systemic approval. The related herbal product chaparral has been associated with serious liver injury and subject to regulatory warning. A topical formulation held an approval for a skin condition.
FDA approval statusNot approved for any systemic indication. Masoprocol, a topical formulation, held an approval for actinic keratoses. Chaparral, the herbal product from the same plant, has been the subject of regulatory warnings over liver injury.
Human studies cited0 of 2 citations on the profile
ReviewedSep 2026

Classification and note come from the NDGA profile, checked against U.S. Food and Drug Administration (FDA) listings at the reviewed date.

What this means

  • 01

    No product containing NDGA is approved by FDA for any use in the United States, so nothing on the market is authorized for people.

  • 02

    "Research use only" is a vendor label, not a legal category that permits human use. It does not exempt a product from medicines law.

  • 03

    Importing, supplying or promoting it for human use can fall under medicines legislation in the United States. This page is general information, not legal advice.

What NDGA is

Extended male mouse lifespan at three different doses, dose-dependently, and never in females. It also causes liver toxicity, which is why the plant it comes from was pulled from the supplement market.

NDGA is a plant lignan from the creosote bush, and it has a rare distinction in lifespan research: its effect was replicated across three separate doses within the same programme, dose-dependently, which very few compounds manage. It is also hepatotoxic, and that is not a theoretical concern.

Mechanism: A lignan with multiple reported activities, which is part of the interpretive problem. It inhibits lipoxygenase enzymes, acts as an antioxidant, and has been reported to affect insulin-like growth factor 1 receptor signalling and mitochondrial function.

Regulatory history: Not approved for any systemic indication. Masoprocol, a topical formulation, held an approval for actinic keratoses. Chaparral, the herbal product from the same plant, has been the subject of regulatory warnings over liver injury.

How FDA treats this kind of product

Approves prescription drugs by indication and polices unapproved products, including peptides sold online. Compounding pharmacies may prepare some compounds under a prescription when the FDA places them on a permitted bulk-substances category.

The classification above is the The Longevity Archive reading of U.S. Food and Drug Administration listings for NDGA at the reviewed date, not a legal opinion. Rules change, and importing, prescribing and possessing a compound can each be treated differently. Check the regulator directly before acting on anything here.

NDGA in other countries

Frequently asked questions

Is NDGA legal in the United States?

No. NDGA is not an approved medicine in the United States; its classification is "Not approved; research use only". Nothing containing it is authorized for any use in people. Vials labeled "for research use only" are not exempt: that label does not make human use lawful. On the evidence, no human study is cited on its profile. Note: No systemic approval. The related herbal product chaparral has been associated with serious liver injury and subject to regulatory warning. A topical formulation held an approval for a skin condition.

Can I buy NDGA in the United States?

No approved product exists to buy. In the United States NDGA is classified as "Not approved; research use only", so there is no licensed pharmacy product. Vendors selling it "for research use only" are not selling it for human use, and that label does not change its legal status. This site does not list or recommend vendors. Note: No systemic approval. The related herbal product chaparral has been associated with serious liver injury and subject to regulatory warning. A topical formulation held an approval for a skin condition.

Is NDGA FDA approved?

No. FDA status: Not approved for any systemic indication. Masoprocol, a topical formulation, held an approval for actinic keratoses. Chaparral, the herbal product from the same plant, has been the subject of regulatory warnings over liver injury.. Current US classification: "Not approved; research use only". On the evidence, no human study is cited on its profile.

Related compounds in the United States

Full research profile

Mechanism, cited studies, FDA status and the full legal summary for NDGA live on its compound profile.

NDGA profile

This page is general information about the regulatory status of NDGA in the United States, current as of Sep 2026. It is not legal advice, and classifications change; check U.S. Food and Drug Administration directly or consult a lawyer for a specific situation. Educational use only. This database summarizes published research. It is not medical advice and contains no dosing protocols or recommendations for personal use. The Longevity Archive has no vendor relationships and does not recommend where to buy anything.