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PABA (Para-Aminobenzoic Acid)

Also called para-aminobenzoic acid, 4-aminobenzoic acid, aminobenzoate potassium, Potaba, vitamin Bx

By Kymata Labs EditorialMedical review pendingLast reviewed October 11, 2026 · What changed

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Summary

PABA is sold as a supplement, but the trials used its potassium salt (Potaba) at 12 g a day. In 75 men with early Peyronie's disease, 12 months shrank plaques and stopped curvature worsening more often than placebo (grade C). In 146 people with scleroderma it did not help the skin. Acute hepatitis has been reported.

Top graded outcomes:C evidence grade Plaque size and curvature in early Peyronie's diseaseC evidence grade Skin thickening and mobility in scleroderma

Key facts

What it is
An aminobenzoic acid; its potassium salt (aminobenzoate potassium, Potaba) is the form tested in trials[1][2]
Peyronie's disease
Response (plaque or curvature) 74.3% on 12 g a day vs 50.0% on placebo after 12 months; plaques shrank, curvature did not worsen[1]
Scleroderma
12 g a day for 48 weeks did not change skin thickening or mobility versus placebo; more people stopped for side effects[2]
Liver
Acute liver injury has been reported in at least six people taking potassium PABA; in the most recent report it resolved after stopping[3]
Evidence base
2 graded human outcomes on this page
Last reviewed
October 11, 2026

How it works

ProposedPotassium PABA is proposed to have antifibrotic effects on connective tissue; how it acts on Peyronie's plaques is not established.[1]

What the human research says

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

At a glance: strongest evidence per outcome

Evidence at a glance: strongest human evidence per outcome
OutcomeGradeEffectStrongest evidenceRows
SclerodermaGrade CNo effectRCT · n = 146 · 1994Form tested: Aminobenzoate potassium1 row
Peyronie's diseaseGrade CImproved74% vs 50% respondersRCT · n = 75 · 2005Form tested: Potassium para-aminobenzoate (Potaba)1 row

Every graded row

Outcome
Form tested
Sort

Showing 2 of 2 outcomes. Human trials only.

OutcomeEffectGradeBest evidencePMID
Skin thickening and mobility in sclerodermaNo effectGrade C

RCT · n = 146 · 1994

Adults with longstanding, stable scleroderma

Form: Aminobenzoate potassium · Dose: 12 g/day · Duration: 48 weeks

No difference from placebo on any outcome; 76 of 146 completed; 18 vs 6 people withdrew for side effects, mostly stomach upset and headache.

8151563 (opens PubMed)Source [2]
Plaque size and curvature in early Peyronie's diseaseImprovedGrade C

RCT · n = 75 · 2005

Men with Peyronie's disease under 12 months, non-calcified plaque (103 randomized)

Form: Potassium para-aminobenzoate (Potaba) · Dose: 12 g/day (3 g four times a day) · Duration: 12 months

Responders 74.3% vs 50.0% on placebo; mean plaque size fell from 259 to 142 mm²; existing curvature did not improve but new or worsening curvature was less common. Pain relief did not differ.

15774254 (opens PubMed)Source [1]

Forms

FormElemental %Absorption (human data)GI toleranceStudied for
Aminobenzoate potassium (Potaba)Varies[1]Not applicable (whole compound or extract; no elemental fraction)No absorption comparison with plain PABA in our sources.[1]Withdrawals for stomach upset and headache were more common than on placebo at 12 g a day; rare acute hepatitis.[2][3]Peyronie's disease, scleroderma (12 g/day)
Para-aminobenzoic acid (supplement form)Varies[1]Not applicable (whole compound or extract; no elemental fraction)No human trials of plain PABA supplements in our sources.[1]No trial data for plain PABA in our sources.[1]Not tested in the trials we cite

Studied doses

Doses studied in human trials ranged from 12 g of potassium aminobenzoate a day, for 48 weeks to 12 months.[1][2]

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

Interactions

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

None found in our sources.

Who should be careful

Liver disease or abnormal liver tests
Acute hepatitis has been reported with potassium PABA; in the latest reported case it resolved about 4 months after stopping.[3]
Anyone self-dosing at trial amounts
The 12 g a day used in trials is a drug-level dose; people withdrew for stomach upset and headache.[1][2]
Pregnancy and breastfeeding
No safety data in the trials we cite.[1][2]

Talk to your pharmacist or clinician before starting a supplement, especially if you take prescription medicines.

Liver safety

Reported with the prescription potassium salt at high doses.

Acute hepatitis
A 2008 report added a case to five earlier ones of acute liver injury with potassium PABA; the patient recovered fully 4 months after stopping.[3]

Frequently asked questions

Is PABA a vitamin?

It is sometimes marketed as “vitamin Bx”, but the human trials tested it as a high-dose drug (the potassium salt), not as a nutrient.[1][2]

Does PABA help Peyronie's disease?

In one placebo-controlled trial, 12 g a day of potassium PABA for 12 months shrank plaques and kept curvature from worsening more often; it did not straighten existing curvature.[1]

Are PABA supplements the same as Potaba?

Potaba is the potassium salt used in the trials, at 12 g a day. Plain PABA supplements have not been tested in those trials.[1][2]

Is PABA safe for the liver?

Acute liver injury has been reported in at least six people taking potassium PABA. Stopping it is the recommended response.[3]

Sources

  1. [1]Potassium paraaminobenzoate (POTABA) in the treatment of Peyronie's disease: a prospective, placebo-controlled, randomized study.. Eur Urol, 2005. RCT PMID 15774254
  2. [2]Comparison of aminobenzoate potassium and placebo in the treatment of scleroderma.. J Rheumatol, 1994. RCT PMID 8151563
  3. [3]Acute hepatitis associated with treatment of Peyronie's disease with potassium para-aminobenzoate (Potaba).. J Sex Med, 2008. review PMID 18624965

What changed

  1. October 11, 2026 · all · new pageFirst draft. Every PMID checked against NCBI E-utilities (title, year and journal taken from the PubMed record) and abstracts read for each cited row. No single-ingredient PABA product was listed by Supersmart US on 2026-10-11, so no product card is shown. Self-reviewed in a second strict pass, then checked by an independent adversarial fact-check against the PubMed abstracts and live product pages. No credentialed medical reviewer yet.Writer: Kymata Labs Editorial · No credentialed reviewer yet

How we write, grade and correct these pages: editorial and evidence policy.

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