Ferulic acid

Also called trans-ferulic acid, 4-hydroxy-3-methoxycinnamic acid, rice bran ferulic acid, sodium ferulate.

The short answer

From 7 sources

Ferulic acid is a phenolic acid abundant in cereal grains. One 6-week Thai trial in 48 adults with high cholesterol found 1,000 mg/day lowered LDL cholesterol by 9.3% and inflammatory markers versus placebo. Oral skin data come from a 16-person company study. Its salt, sodium ferulate, induced a drug-metabolising enzyme in a human study. Evidence is limited.

Key facts

Cholesterol
1,000 mg/day for 6 weeks lowered total cholesterol 8.1%, LDL 9.3% and triglycerides 12.1%, and raised HDL 4.3%, versus placebo in 48 adults with high cholesterol1
Inflammation markers
In the same trial hs-CRP fell 32.7% and TNF-alpha 13.1% versus placebo1
Skin (oral)
200 mg/day for 2 weeks reduced water loss through the skin from baseline in a 16-person pilot run by a consumer-goods company2
Drug metabolism
Two weeks of sodium ferulate induced CYP2B6 metabolism of the antidepressant bupropion in 33 healthy people, with the effect varying by genotype5
Food sources
Ferulic acid is the most abundant phenolic compound in vegetables and cereal grains1

What it is

Ferulic acid is a plant phenolic acid found in cereal bran and vegetables, sold as an oral supplement and used in topical skin serums.

How it works

Proposed

Ferulic acid is an antioxidant phenolic acid; laboratory and animal studies report lipid-lowering, antioxidant and anti-inflammatory effects. In the human cholesterol trial, the oxidative-stress marker MDA and oxidized LDL fell. Whether these effects explain the lipid changes is unproven.1

Forms, side by side

3 forms named in our sources. The rest show what our data holds, and say plainly where it holds nothing yet.

Ferulic acid forms compared

3 forms
Ferulic acid forms compared: 3 forms by 3 attributes. Empty cells are labelled No data yet, or Not graded in the evidence row.
3 formsCapsules (often from rice bran)Sodium ferulate (drug salt)Topical ferulic acid (solutions and serums)
Absorption in peopleNo absorption data in the cited abstracts.1Induced CYP2B6 drug metabolism after 14 days in healthy people.5Applied to skin; not a source of oral intake.4
GI toleranceNo adverse effects reported in the cited abstracts at 200-1,000 mg/day for 2-6 weeks.12Adverse events were reported in only 6 of 36 trials in the meta-analysis.6Initial greasy feel; tingling and itching in one of 30 users.4
Studied forCholesterol, skin barrierCoronary heart disease (as a medicine in China)Rosacea (with doxycycline); skin dullness (1% cream, exploratory split-face study led by a rice-bran ferulic acid maker, Tsuno Rice Fine Chemicals)
  1. Ferulic acid capsules (often from rice bran)
    Absorption in people
    No absorption data in the cited abstracts.1
    GI tolerance
    No adverse effects reported in the cited abstracts at 200-1,000 mg/day for 2-6 weeks.12
    Studied for
    Cholesterol, skin barrier
  2. Sodium ferulate (drug salt)
    Absorption in people
    Induced CYP2B6 drug metabolism after 14 days in healthy people.5
    GI tolerance
    Adverse events were reported in only 6 of 36 trials in the meta-analysis.6
    Studied for
    Coronary heart disease (as a medicine in China)
  3. Topical ferulic acid (solutions and serums)
    Absorption in people
    Applied to skin; not a source of oral intake.4
    GI tolerance
    Initial greasy feel; tingling and itching in one of 30 users.4
    Studied for
    Rosacea (with doxycycline); skin dullness (1% cream, exploratory split-face study led by a rice-bran ferulic acid maker, Tsuno Rice Fine Chemicals)
Every cell holds data from a cited page; citation numbers link to the page that holds them.Scroll the table for every column

What the human research says

Human trials only, one row per outcome. The form line shows what each trial actually tested. Grades follow our evidence-grading policy.

Trial map

4 graded outcomes, largest study first

All 4 graded outcomes found an improvement. The largest, a 2023 meta-analysis of 3,207 people on clinical response in coronary heart disease (sodium ferulate added to standard drugs), found an improvement.

1Clinical response in coronary heart disease (sodium ferulate added to standard drugs)

Improved · Grade C · Meta-analysis, 3,207 people, 2023

Patients with coronary heart disease in Chinese randomized trials

Dose, result and source
Every graded outcome on this page, largest study first
OutcomeFoundPeopleStudyWho was studied
Clinical response in coronary heart disease (sodium ferulate added to standard drugs)Improved3,207Grade C · Meta-analysis, 2023Patients with coronary heart disease in Chinese randomized trials
Rosacea lesions with topical ferulic acid added to doxycyclineImproved60Grade C · RCT, 2025Chinese adults with mild-to-moderate papulopustular rosacea
LDL, total cholesterol and triglyceridesImproved48Grade C · RCT, 2018Thai adults with high blood lipids
Skin barrier (water loss and hydration)Improved16Grade D · Pilot RCT, 2023Healthy Japanese men
Each circle is one graded outcome on this page, numbered from the largest study down, and placed by how many people it studied (log scale). It shows who was studied and what was found, not advice about your dose.

Every graded row

4 rows

Showing 4 of 4 outcomes. Human trials only.

Grade CClinical response in coronary heart disease (sodium ferulate added to standard drugs)Heart disease (drug form)RR 1.21, low-quality evidenceMeta-analysis · 36 studies
n 3,207 · 2023

Improved Added to conventional drugs, sodium ferulate improved overall clinical effectiveness (RR 1.21) and several ECG, angina and inflammatory measures, but most outcomes were rated low or very low quality evidence.

Design
Meta-analysis, 36 studies, n = 3,207, 2023
Population
Patients with coronary heart disease in Chinese randomized trials
Form
Sodium ferulate (a drug derivative of ferulic acid) plus conventional drugs
Dose
Varied by trial
Duration
Varied by trial
Source
Reference 6 · PubMed 37116387 (opens PubMed)
Grade CRosacea lesions with topical ferulic acid added to doxycyclineSkin80% vs 63% respondersRCT
n 60 · 2025

Improved Lesion and self-assessment scores improved more than with saline; overall response 80.0% vs 63.3%. One person reported tingling and itching; no serious adverse reactions.

Design
RCT, n = 60, 2025
Population
Chinese adults with mild-to-moderate papulopustular rosacea
Form
Topical ferulic acid solution vs saline, both with oral doxycycline
Dose
Applied twice daily (with doxycycline 0.1 g/day)
Duration
6 weeks
Source
Reference 4 · PubMed 39413013 (opens PubMed)
Grade CLDL, total cholesterol and triglyceridesCholesterolLDL -9.3% vs placeboRCT
n 48 · 2018

Improved Versus placebo: total cholesterol -8.1%, LDL -9.3%, triglycerides -12.1%, HDL +4.3%; oxidized LDL -7.1%, MDA -24.5%, hs-CRP -32.7% and TNF-alpha -13.1%.

Design
RCT, n = 48, 2018
Population
Thai adults with high blood lipids
Form
Ferulic acid capsules
Dose
1,000 mg/day
Duration
6 weeks
Source
Reference 1 · PubMed 29865227 (opens PubMed)
Grade DSkin barrier (water loss and hydration)SkinLess water loss vs baselinePilot RCT
n 16 · 2023

Improved Transepidermal water loss fell from 6.1 to 4.8 g/m2/h and hydration rose from 30.1 to 32.3 units versus baseline; the change in sympathetic nerve activity differed from placebo.

Design
Pilot RCT, n = 16, 2023
Population
Healthy Japanese men
Form
Ferulic acid capsules
Dose
200 mg/day
Duration
2 weeks
Source
Reference 2 · PubMed 33973806 (opens PubMed)

Memory and brain health: animal studies only

1 note
Cognition (animal studies)
A 2024 systematic review searched the literature through October 2023 and found no human studies of ferulic acid and cognitive function. All 26 eligible studies were in animals, most in dementia models, where ferulic acid lessened induced cognitive decline. Whether that applies to people is untested.7

What the numbers add up to

Each point is worked out from the data and the sources numbered on this page, with the arithmetic shown under it. It adds no new data and is not medical advice.

One oral efficacy trial

The lipid results come from a single 48-person, 6-week trial; no independent replication was found.1

How we got this: Evidence table on this page

Studied doses

Doses used in research, shown against the official limits. They describe the studies, not a recommendation for you.

Studied doses in research, not advice. These are amounts used in research, not personal advice. Your clinician or pharmacist can say what fits you.

Doses studied in human trials

Doses studied in human trials ranged from 200 mg/day for 2 weeks to 1,000 mg/day for 6 weeks of oral ferulic acid. These are research doses, not recommendations.21

Interactions and safety

Published interactions only: each row cites a source. No row means none was found in our sources, not that a combination is safe.

What Ferulic acid meets

1 cited row

Medicines 1

Ferulic acid1 medicine · 0 supplements

Supplements and foods 0

No supplement rows in our sources.

  • Measured in a human study
Rows as our evidence profiles cite them; links stay on this site. Line weight shows what backs a row, not how serious an interaction is. No line means none was found in our sources, not that a combination is safe. Not medical advice: ask your pharmacist.

Interactions

1 agent
Published interactions, grouped by kind
AgentWhat the source saysEvidence
Medicines1
Drugs metabolised by CYP2B6e.g. BupropionSodium ferulate taken for 14 days induced CYP2B6 hydroxylation of bupropion in healthy volunteers, with the size of the effect depending on PXR and CYP2B6 genotype. Whether ferulic acid supplements do the same is untested.5PK study

Check with what you take

Kept on this device only

Add what you take. We list every interaction our evidence profiles cite between Ferulic acid and your picks, and between your picks.

Most cited:

Add a supplement or medicine you take to check it against Ferulic acid.

Starting from one medicine? The interaction checker rates how serious each pair is, on a curated list of 19 entries for 11 medicines. This cabinet has no severity rating: it lists every interaction row our supplement pages cite.

Not medical advice, and no dosing advice. An empty result means no row we cite names that pair, by name or through a drug class we can link the medicine to, not that a combination is safe. Where our sources name only a group of medicines we cannot match, the cabinet says so. Ask your pharmacist before you combine supplements and medicines.

Who should be careful

3 groups
People taking bupropion or other CYP2B6-metabolised drugs
Sodium ferulate changed how the body processes bupropion in a human study; ask a pharmacist before combining.5
Pregnancy and breastfeeding
The cited trials enrolled non-pregnant adults only, so there are no safety data for supplement doses in pregnancy or breastfeeding.12
Sensitive skin (topical products)
In a rosacea trial, topical ferulic acid caused a greasy feel at first and tingling and itching in one user.4
Talk to your pharmacist or clinician before starting a supplement, especially if you take prescription medicines.

How to read the label

What to check on the Supplement Facts panel.

How to read the label

2 checks
Oral vs topical

Skin serums pair ferulic acid with vitamins C and E for use on the skin. The cholesterol trial tested 1,000 mg/day swallowed as capsules, a different use.14

Ferulic acid vs sodium ferulate

Sodium ferulate is the salt used as a medicine in China; most of the heart-disease trials and the drug-interaction study used it, not supplement capsules.56

Frequently asked questions

Short answers to common questions; the numbers link to the sources below.

Common questions

6 answers
Does ferulic acid help memory or brain health?

There is no human evidence. A 2024 systematic review found no human studies of ferulic acid and cognition; its 26 included studies were all in animals, mostly in dementia models.7

Does ferulic acid lower cholesterol?

In one 6-week trial of 48 adults with high cholesterol, 1,000 mg/day lowered LDL by 9.3% versus placebo. That has not been replicated.1

Does taking it by mouth help skin?

A 16-person, 2-week pilot run by a consumer-goods company found less water loss through the skin than at baseline. That is too small to judge.2

Is ferulic acid safe to take?

No one reported side effects in the 6-week, 1,000 mg/day cholesterol trial (48 people, per its full text); the 2-week skin pilot's abstract does not mention them. Both trials were small and short. Safety beyond 6 weeks, in pregnancy and with medicines is unstudied, and the drug salt sodium ferulate changed how bupropion is metabolised.125

Does ferulic acid interact with medicines?

Its salt, sodium ferulate, sped up the CYP2B6 metabolism of bupropion in a human study. Supplement capsules have not been tested for this.5

Is topical ferulic acid the same as the supplement?

No. Topical products act on the skin; a rosacea trial applied a ferulic acid solution alongside oral doxycycline. Oral and topical results should not be mixed.4

What changed

Every dated change to this page: what changed, who made it and why.

Change log

2 entries
Dated changes to this page
DateChangeWho and why
evidence notes, FAQ, questions, relatedRe-ran the PubMed search for ferulic acid trials and reviews (through October 2026): no new oral human trial or meta-analysis qualified for the table. Added a 2024 systematic review showing there are no human studies of ferulic acid and memory or cognition (animal studies only) as a research note. Replaced the FAQ item that repeated the page's own "What is" question with memory and safety answers, added page questions and goal-hub links. Checked LactMed, LiverTox, NCCIH and MedlinePlus: none has a ferulic acid entry, so the pregnancy note still rests on the trials' enrolment (no data) and the only interaction remains the sodium ferulate–bupropion study. Topical vitamin C/E/ferulic serum trials were not added (combination products).Writer: Kymata Health EditorialTrigger: A–Z audit against docs/supplements/AUDIT-STANDARD.md
allInitial editorial evidence review (first draft). Every PMID checked against NCBI E-utilities esummary (titles and years taken from the record, none retracted) and the abstract read for each cited row. Studied doses are reported as research doses, not dosing advice.Writer: Kymata Health EditorialTrigger: new page

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