Knowledge · Natural Compounds

Niacinamide

Database-based evaluation · 162 studies in our database, 25 of them controlled human trials · As of · How we work

Niacinamide is the amide form of vitamin B3; human studies suggest benefits especially for the skin, otherwise the situation is unclear.

We evaluated 71 human studies on Niacinamide, including 25 randomised controlled trials and 3 meta-analyses or systematic reviews; the controlled studies include 2,588 participants in total. As of 16 October 2026.

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1. What Is Niacinamide? Occurrence, Origin and Forms

Niacinamide is the amide form of vitamin B3 (niacin) and belongs to the water-soluble vitamins. It occurs in animal and plant foods and is also formed in the body from the amino acid tryptophan. It is used as a vitamin supplement and as an ingredient in skin care products.

Niacinamide is found in meat, fish, milk, eggs, legumes and cereals. In skin care it is applied topically to the skin.

For supplements and skin care, niacinamide is produced industrially; in foods it occurs naturally. In human studies, mainly oral forms (tablets, capsules) and topical preparations (cream, gel, serum) are examined.

Forms and Preparations Studied

  • Oral form (tablets, capsules, powder)
  • Topical preparation (cream, gel, serum, lotion)
  • Fortified foods and beverages
  • Injection solution
  • Combination products with other B vitamins

Not covered on this page:

  • Nicotinic acid (niacin) – a different form of vitamin B3 with its own properties
  • Nicotinamide riboside and nicotinamide mononucleotide (NMN) – separate substances studied as NAD+ precursors
  • NAD+ itself and infusions of it
  • Tryptophan – an amino acid from which the body can form niacinamide

2. What Does Niacinamide Do? Results by Area

AreaResult in controlled studiesStrength of evidenceStudiesParticipants
Skin (acne, pigmentation, skin barrier)mixedmoderate0 meta-analyses · 5 controlled · 36 other267
Kidney and dialysismostly improvedlow0 meta-analyses · 1 controlled · 2 other26
Skin cancer and precursor lesionsmixedunclear0 meta-analyses · 1 controlled · 3 other26
Joints and inflammationmixedunclear0 meta-analyses · 1 controlled · 1 other90
Niacin deficiency (pellagra)reviews onlyunclear0 meta-analyses · 0 controlled · 1 other0
Blood sugar and diabetesobservational data onlyunclear0 meta-analyses · 0 controlled · 1 other0
Other investigationsobservational data onlyunclear0 meta-analyses · 0 controlled · 8 other0

How to read the table: counted are human studies whose results concern the area. “High” means at least one meta-analysis and two controlled studies showing improvement, or at least three controlled studies of which three quarters show improvement, with at least 300 participants in total. “Moderate” means at least two controlled studies showing improvement, as a majority, or one meta-analysis alongside controlled studies. “Low” means one controlled study showing improvement. Where an area has no controlled study, the strength of evidence is at most “low” (result “reviews only” or “observational data only”). Everything else is “unclear”. A study counts as showing improvement when at least half of its outcomes in this area improved. Reviews of combination products do not count as meta-analyses; results that only describe side effects or shares of users do not count as an effect. The same study is counted only once.

3. What the Studies Show in Detail

Niacinamide and Skin (Acne, Pigmentation, Skin Barrier): Human Studies

In acne, a systematic review, based on a single randomized trial, found lower sebum production with topical nicotinamide 1. For dark discolorations of the armpits, a systematic review counts topical niacinamide among the effective agents 2. A systematic review of natural active substances counts niacinamide, alongside azelaic acid, soy, arbutin, licorice and others, among the agents with a lightening effect in hyperpigmentation 5. In women with aged skin, a niacinamide formulation in a placebo-controlled trial improved stratum corneum moisture, water loss and sebum content; ultrasound alone brought no measurable improvement 13. In mild atopic dermatitis, niacinamide-containing body lotions, partly with cleansing gel, improved SCORAD, itching, quality of life and skin barrier more than in the control group; all received ebastine 8. In discoid lupus erythematosus, the skin lesions in a placebo-controlled trial responded better to 4% nicotinamide than to 2%, with more irritation 15. Against skin redness triggered by retinol, 3% niacinamide did not help in a placebo-controlled patch test 21. In acne, niacinamide as an addition to benzoyl peroxide lowered the non-inflammatory lesions more than benzoyl peroxide alone, but not the inflammatory ones 22. Investigated were predominantly topical preparations such as cream, gel and serum; the evidence is moderate, because the controlled trials are small, short and turned out mixed.

StudyDesign · participantsPreparation · dose · duration · comparisonResult
1 Althwanay et al. 2024review · 41 participantsTopical niacinamide; vs. Randomized controlled trial (comparator not reported)Sebum production: improved
2 Vahabi et al. 2025reviewTopical niacinamide, among desonide, HQ, AHA, herbal extracts; vs. Laser/light therapies and other topical agentsPigmentation reduction: improved
3 Speeckaert et al. 2023systematic reviewNiacinamide as antioxidant; vs. Baseline vs. follow-up (MASI)Pigmentation (melasma): improved
4 González-Molina et al. 2022reviewTopical niacinamide as adjuvant; vs. Hydroquinone and triple combination therapyEfficacy in melasma: improved
5 Hollinger et al. 2018systematic reviewNiacinamide as one of several natural depigmenting agents; vs. other natural ingredients or controlsDepigmenting efficacy in hyperpigmentation: improved
8 Zhu et al. 2023randomised controlled · 122 participantsNiacinamide-containing body emollients, with or without cleansing gel; 28 days; vs. Placebo control; all groups also received oral ebastine 10 mg/daySCORAD score: improved (12.43 ± 3); Peak pruritus NRS: improved (3.3 ± 0.9); DLQI score: improved (7.1 ± 2.33)
13 Vergilio et al. 2025randomised controlled · 67 participantsTopical niacinamide formulation (cosmetic) vs. placebo; 8 weeks, 8 sessions of 5-US (weekly, 20 min); vs. Placebo formulation, placebo + 5-US, formulation + 5-USstratum corneum aqueous content: improved; transepidermal water loss: improved; sebum reduction: improved
15 Nouh et al. 2023randomised controlled · 60 participantsTopical nicotinamide 2% and 4% as cream and gel; 2% and 4% nicotinamide; vs. Cream/gel base as placebo controlResponse of DLE skin lesions: unclear; Response 4% vs. 2% nicotinamide: improved; Irritation with 4% vs. 2% nicotinamide

Further studies in this area: 21 22 26 27 28 29 30 31 32 33 34 37 39 40 41 42 43 45 46 47 48 49 50 51 52 53 55 56 57 58 59 60 61

Niacinamide, Kidney and Dialysis: Human Studies

In adults on hemodialysis, orally taken nicotinamide as an addition to phosphate binders lowered the serum phosphate level more than placebo; in the analysis of all randomized participants, the difference was similar but not confirmed 19. This is the only controlled study in this area; it was double-blind, randomized and of crossover design, included 26 evaluable participants and lasted only a short time, so the evidence is weak 19. In an observational study of Chinese adults, the blood level of niacinamide was among several metabolic markers that predicted newly occurring chronic kidney disease; intake was not investigated 24. A review on polycystic kidney disease classifies the benefit of niacinamide, like that of curcumin or vitamin E, as uncertain and advises against such supplements 54. Thus, the efficacy and safety of oral administration in dialysis patients over longer periods remain open.

StudyDesign · participantsPreparation · dose · duration · comparisonResult
19 Schepers et al. 2024randomised controlled · 26 participantsOral niacinamide (NAM) as add-on to phosphate binders; 250-500 mg/day; 12 weeks per treatment arm (crossover); vs. Placebo, double-blind, randomized, crossoverSerum phosphate (per-protocol): improved (reduced serum phosphate with 0.59 mg/dL (p = .03)); Serum phosphate, between-treatment difference (linear mixed-effects model): improved (0.77 mg/dL (95% CI 0.010, 1.43; P = .03)); Serum phosphate (intention-to-treat): no difference
24 Liu et al. 2025cohort study · 3,802 participantsniacinamide as circulating metabolite (LC-MS metabolomics); follow-up 4.6 ± 0.2 years; vs. participants without vs. with incident CKDniacinamide as predictor of incident CKD (LASSO panel of 8 metabolites): unclear (OR 8.79 (95 % CI: 7.49, 10.32; P < 0.001))
54 Chebib et al. 2024reviewNiacinamide as supplement, mentioned among other substances; vs. no comparison reportedClinical benefit in ADPKD: unclear (uncertain clinical benefit)

Niacinamide, Skin Cancer and Precursor Lesions: Human Studies

For skin cancer and its precursors, the evidence is unclear. A randomized controlled trial in 26 patients with actinic keratosis lesions compared a topical niacinamide gel with topical fluorouracil and found fewer treatment complications such as burning, itching and erythema with niacinamide, while fluorouracil was superior in improvement according to photography and dermatoscopy as well as from the patient's perspective 18. Review articles report that non-melanoma skin cancer occurred less frequently with oral nicotinamide 51, describe topical preparations for actinic keratosis 53 and consider vitamin B3 promising for the prevention of non-melanoma skin cancer 57. The studies differ greatly in form, dose, duration and comparator, and the controlled evidence relies on a very small sample.

StudyDesign · participantsPreparation · dose · duration · comparisonResult
18 Poostiyan et al. 2025randomised controlled · 26 participants1% niacinamide topical gel; twice daily; 3 months; vs. 5% fluorouracil topical cream twice daily for 4 weeksimprovement by photography and dermoscopy: unclear; patients' perspectives: unclear; treatment complications (burning, itching, erythema)
51 Shoukfeh et al. 2025reviewOral nicotinamide; vs. low versus high dosesIncidence of non-melanoma skin cancers: improved
53 Ong et al. 2024reviewTopical niacinamide in various formulationsTreatment of actinic keratosis: improved
57 Elgharably et al. 2023reviewNiacinamide and other B vitamins (B2, B6, B12, folic acid); vs. no uniform comparisonNonmelanoma skin cancer prophylaxis: improved

Niacinamide, Joints and Inflammation: Human Studies

For joints, only one randomized trial is available: in knee osteoarthritis, a hyaluronic acid preparation with niacinamide was compared with another hyaluronic acid preparation; only stiffness improved more 11. A case series with intra-articular hyaluronic acid injections plus niacinamide reported pain reduction, among others in meniscal damage, without a relationship to the radiological or MRI severity 44. Since niacinamide was given in both investigations only as a component of a mixture with hyaluronic acid, no effect can be attributed to niacinamide alone. The overall strength of evidence is unclear: there is no meta-analysis, and the only controlled study is small and limited to one injection form. For oral or topical niacinamide forms for joint complaints, controlled studies in this area are lacking.

StudyDesign · participantsPreparation · dose · duration · comparisonResult
11 Hofweber et al. 2024randomised controlled · 90 participantsINNORYOS 2.2% hyaluronic acid containing 15 mg niacinamide; 15 mg niacinamide per injection; 26 weeks, injections at baseline, week 1 and 2; vs. Synvisc 0.8%, 2.0 mlWOMAC pain score: unclear (p = .26); WOMAC stiffness subscale: unclear (p = .009); WOMAC function score: unclear (p = .49)
44 Pennekamp et al. 2024case seriesIntra-articular hyaluronic acid injections with niacinamide; vs. Subgroups by injection frequency (1, 2, >2)Pain reduction on numeric rating scale (NRS 0-10): improved (mean decrease of 3.34 ± 1.65); Pain reduction between 1 and 2 injections: improved (p = 0.027); Pain reduction between 1 and >2 injections: improved (p = 0.032)

Niacinamide and Niacin Deficiency (Pellagra): Human Studies

For pellagra, only one review article is available; it describes the treatment of pellagra with vitamin B3 as an early, historically documented benefit 58. Since the review treats nicotinic acid and nicotinamide together as niacin, the finding cannot be attributed to nicotinamide alone 58. Controlled studies on the treatment of pellagra with niacinamide were not found in this evaluation; the strength of evidence is therefore unclear. It remains open which form, dose and duration are effective for the treatment of pellagra.

StudyDesign · participantsPreparation · dose · duration · comparisonResult
58 Epstein et al. 2023reviewNiacin/niacinamide, also topicalpellagra treatment: improved

Niacinamide, Blood Sugar and Diabetes: Human Studies

For blood sugar and diabetes, no controlled trial on niacinamide is available; the strength of evidence is unclear. An observational study (cross-sectional) in Chinese adults found that diabetics with higher plasma levels of niacin had hyperlipidemia, hypercholesterolemia and hypertriglyceridemia less frequently 25. Blood levels of nicotinamide and nicotinic acid were measured, not an intake; the association also held for nicotinamide alone 25. Since it is a cross-sectional observation, no cause-and-effect relationship can be derived from it. It remains open whether oral or topical niacinamide administration influences blood sugar or diabetic metabolic consequences.

StudyDesign · participantsPreparation · dose · duration · comparisonResult
25 Geng et al. 2024cross-sectional study · 2,647 participantsPlasma niacinamide/nicotinic acid (endogenous measurement); vs. highest vs. lowest quartile of plasma niacinhyperlipidemia risk in diabetic participants: improved (54%, 50%, and 52% lower risk); hypercholesterolemia in diabetic participants: improved (0.54 (0.38, 0.77)); hypertriglyceridemia in diabetic participants: improved (0.61 (0.44, 0.85))

Niacinamide: Further Outcomes in Studies

In this area, mainly observations and individual controlled studies on oral nicotinamide were examined, not on topical application. A randomized controlled trial in adults on hemodialysis found no difference in platelet count with oral administration as an addition to phosphate binders 19. A single-arm study in glaucoma patients reported better vision-related quality of life after oral niacinamide, without a control group 23. Observational studies found no increased risk of serious cardiovascular events with oral nicotinamide 38 and less frequent heart attacks 35. The studies are small, uncontrolled or only observational; the overall strength of evidence is unclear.

StudyDesign · participantsPreparation · dose · duration · comparisonResult
19 Schepers et al. 2024randomised controlled · 26 participantsOral niacinamide (NAM) as add-on to phosphate binders; 250-500 mg/day; 12 weeks per treatment arm (crossover); vs. Placebo, double-blind, randomized, crossoverPlatelet counts; Drop-outs due to side effects (3 drop-outs due to side effects (8.6%))
23 Nicola et al. 2025case series · 58 participantsoral niacinamide (B3); 500 mg daily; 6 months; vs. no control (single-arm, before-after)Quality of life (GQL-15 total score): improved (mean difference = -2.10, 95% CI: [-2.89, -1.32], p < 0.0001); Central and near vision (GQL-15): improved (mean difference = -2.16, 95% CI: [-3.91, -0.4], p = 0.017); Peripheral vision (GQL-15): improved (mean difference = -2.66, 95% CI: [-0.23, -0.08], p < 0.001)
33 Clark-Loeser et al. 2025case series · 7 participantsTopical cysteamine-isobionicamide formula; once daily; 16 weeks; vs. no control (case series)quality of life: improved (significant improvement)
35 Salem et al. 2026cohort studyoral niacinamide; ≥ 500 mg; 3 years; vs. niacinamide-naive controls (1:1 matched)ST elevation myocardial infarction: improved (RR: 0.547, 95% CI: 0.349-0.858, P = .008); peripheral vascular disease: improved (RR: 0.741, 95% CI: 0.605-0.909, P = .004); cardiac arrest: improved (RR: 0.500, 95% CI: 0.275-0.909, P = .020)
36 Nicola et al. 2026studyoral niacinamide (nicotinamide, vitamin B3); 500 mg daily; 6 months; vs. no control arm; comparison to baselineVisual field Mean Deviation (MD): no difference (mean ΔMD +0.43 dB; GEE p = 0.099; LME p = 0.101); Pattern Standard Deviation (PSD): no difference (PSD remained stable); peripapillary retinal nerve fiber layer (RNFL) thickness: worsened (-1.26 µm; GEE p = 0.046)
38 Wheless et al. 2025cohort studynicotinamide; vs. nicotinamide-exposed vs unexposed patientsMACE incidence: no difference; MACE hazard ratio without prior MACE (VUMC): no difference (HR, 2.02; 95% CI, 0.81-5.05); MACE hazard ratio with prior MACE (VUMC): improved (HR, 0.46; 95% CI, 0.22-0.95)
51 Shoukfeh et al. 2025reviewOral nicotinamide; vs. low versus high dosesMajor adverse cardiovascular effects
58 Epstein et al. 2023reviewNiacin/niacinamide, also topicalCOVID-19 adjunctive treatment: unclear

4. How Is Niacinamide Dosed? Preparation, Dose and Duration in Studies

The studies predominantly used topical preparations such as cream, gel and serum, as well as oral forms as tablets or capsules and an injection solution into the knee joint. Many topical investigations tested niacinamide as a component of a mixture with other active substances such as salicylic acid, tranexamic acid or hyaluronic acid. The doses and durations of use are shown in the table.

Preparation or formDoseDurationStudy
30% SSA combined with 10% niacinamide vs. placebo30% SSA + 10% niacinamide16 weeks6
Dermocosmetic cream with niacinamide et al. plus adapalene 0.1% cream—8 weeks7
Niacinamide-containing body emollients, with or without cleansing gel—28 days8
Dermocosmetic containing salicylic acid, niacinamide, and thermal spring water—Phase 1: 12 weeks; Phase 2: 12 weeks9
Niosomal TXA 2%/NCA 2% cream or conventional TXA 5%/NCA 4% creamTXA 2%/NCA 2% or TXA 5%/NCA 4%three months10
INNORYOS 2.2% hyaluronic acid containing 15 mg niacinamide15 mg niacinamide per injection26 weeks, injections at baseline, week 1 and 211
Liquid botanical nutraceutical containing niacinamide and other ingredients60 mL twice daily90 days12
Topical niacinamide formulation (cosmetic) vs. placebo—8 weeks, 8 sessions of 5-US (weekly, 20 min)13
Serum B3 (5% niacinamide) vs. 4% hydroquinone5% niacinamide in serum5 months Serum B3; HQ4% 3 months then 2 months Serum B314
Topical nicotinamide 2% and 4% as cream and gel2% and 4% nicotinamide—15
Ceramide and niacinamide-containing moisturizer (CCM) vs. hydrophilic cream—8 weeks16
Topical emollient containing panthenol, niacinamide, and dipotassium glycyrrhizatetwice daily28 days17
1% niacinamide topical geltwice daily3 months18
Oral niacinamide (NAM) as add-on to phosphate binders250-500 mg/day12 weeks per treatment arm (crossover)19
Cosmetic serum containing niacinamide, postbiotics and peptides—4 weeks20

5. Is Niacinamide Safe? Side Effects in Studies

In the studies, niacinamide was predominantly well tolerated, with minor local side effects 15; burning, itching and redness occurred less often than with fluorouracil 18. With oral administration to dialysis patients, there were individual discontinuations due to side effects 19. A review warns against a possible cardiovascular risk from breakdown products at high oral doses 51; large observational studies found no increased risk of serious cardiovascular events 3538. A higher topical concentration was associated with more irritation 15.

StudyReported side effects
2 Vahabi et al. 2025Desonide and C. rotundus oil with minimal side effects; laser more painful
4 González-Molina et al. 2022Minimal side effects
6 Xiong et al. 20241 drug-related AE and 1 drug-unrelated AE in the SSA group; no AE in the placebo group
7 Sitohang et al. 2024Better tolerability in Groups B and C
8 Zhu et al. 2023No obvious adverse reactions
9 Khammari et al. 2023good tolerance
10 Ghasemiyeh et al. 2025Less serious adverse reactions than hydroquinone; relapse observed in hydroquinone group
11 Hofweber et al. 2024No adverse effects observed or reported
12 Messier et al. 2026No adverse events reported
14 Rocio et al. 2025Higher erythema in HQ group; Serum B3 better tolerated
15 Nouh et al. 20234% had higher irritation incidence; overall minimal side effects
16 Tempark et al. 2024No serious side effects from either cream

6. What Remains Open: Limits of the Evidence

  • Many skin studies are small and short, and niacinamide was often tested only as part of a mixture.
  • For kidney, joints, blood sugar and pellagra, robust controlled studies are lacking.
  • Findings on topical use cannot be transferred to oral forms and vice versa.
  • Little is known about the long-term safety of oral administration in dialysis patients.
  • Whether niacinamide prevents skin cancer cannot be assessed from the available studies; for the treatment of actinic keratosis there is only one small comparative study.

7. Bottom Line: What Is Established About Niacinamide

Niacinamide is the amide form of vitamin B3 and is used both orally and topically.

On the skin, niacinamide-containing preparations improved the skin barrier in small controlled studies 813, but did not alleviate redness triggered by retinol 21. In other areas, the evidence is weak. In hemodialysis, oral nicotinamide in addition to phosphate binders lowered the serum phosphate level more than placebo; in the analysis of all randomized participants, the difference was not confirmed 19. For joints, blood sugar and precancerous skin lesions, the available studies are insufficient for an assessment 1118; for pellagra, only a review is available 58. Tolerability was predominantly good in the studies, with local irritation as the most common side effect 15.

Frequently Asked Questions

How well has Niacinamide been studied in humans?

We evaluated 71 human studies on Niacinamide, including 25 randomised controlled trials and 3 meta-analyses or systematic reviews; the controlled studies include 2,588 participants in total. As of 16 October 2026.

Does Niacinamide help with skin (acne, pigmentation, skin barrier)? What the studies show

We evaluated 5 controlled studies and 36 further studies; the controlled studies include 267 participants in total. Result of the controlled studies: mixed. Strength of evidence under our published rules: moderate. Sources: 1234

Does Niacinamide help with kidney and dialysis? What the studies show

We evaluated one controlled study and 2 further studies; the controlled studies include 26 participants in total. Result of the controlled studies: mostly improved. Strength of evidence under our published rules: low. Sources: 192454

Does Niacinamide help with skin cancer and precursor lesions? What the studies show

We evaluated one controlled study and 3 further studies; the controlled studies include 26 participants in total. Result of the controlled studies: mixed. Strength of evidence under our published rules: unclear. Sources: 18515357

Does Niacinamide help with joints and inflammation? What the studies show

We evaluated one controlled study and one further study; the controlled studies include 90 participants in total. Result of the controlled studies: mixed. Strength of evidence under our published rules: unclear. Sources: 1144

What is niacinamide and how does it differ from nicotinic acid?

Niacinamide is the amide form of vitamin B3 and belongs to the water-soluble vitamins. Nicotinic acid is another form of vitamin B3 with its own properties and its own studies. Findings on nicotinic acid cannot be transferred to niacinamide.

What effect do human studies show on the skin?

For acne, topical nicotinamide reduced sebum production according to a systematic review, based on a single randomized trial 1. For dark discolorations of the armpits, a systematic review counts topical niacinamide among the effective agents 2. For melasma, topical niacinamide is considered an effective adjunct treatment according to a systematic review 4.

How well is niacinamide tolerated?

In the studies, niacinamide was predominantly well tolerated. Local side effects were minor 15; burning, itching and redness occurred less often than with fluorouracil 18. A higher topical concentration was associated with more irritation 15.

Are there studies on oral niacinamide in kidney disease?

In adults on hemodialysis, orally taken nicotinamide as an addition to phosphate binders lowered the serum phosphate level 19. The study was small and short, the evidence is weak.

What should be considered with combination products?

A benefit then cannot be attributed to niacinamide alone. Such findings apply only to the mixture studied.

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Every statement on this page carries its evidence tier — proven, plausible or hypothesis — and leads to the original work. The decision in the individual case rests with the practitioner; we provide the connections.

International Health Research · https://ih-research.com/en/knowledge/niacinamide/ · Last updated: 2026-10-16