Chronic non-bacterial prostatitis (CP/CPPS) doesn't respond reliably to antibiotics. The 2025 AUA guideline update recognizes phytotherapy as part of the evidence base for CP/CPPS management — that's the territory Pro-UROL was built for.
Formulation rationale
Each active is included at a dose informed by published research on its respective compound class — not an arbitrary "proprietary blend" amount.
Quercetin400 mg (as Quercetin dihydrate)
A bioflavonoid evaluated in clinical studies for chronic pelvic pain symptom scores (NIH-CPSI). Included at 400 mg — the dose used in published CP/CPPS trials — for its anti-inflammatory and antioxidant properties within prostate tissue.
Pollen Extract120 mg (Secale cereale, 10:1, equivalent to 1,200 mg dry)
Cernitin-type rye pollen extracts are among the most studied botanicals for CP/CPPS, with multiple controlled trials assessing pelvic pain and urinary symptom scores over 12–24 weeks. Standardized 10:1 extract ensures consistent potency.
Papain100,000 FCC PU (equivalent to 50 mg, Carica papaya — Fruit)
A proteolytic enzyme derived from papaya fruit, included for its systemic anti-inflammatory activity. Enzyme activity is measured in FCC PU (Food Chemicals Codex Papain Units) to ensure consistent potency across batches.
Stem Bromelain1,200,000 FCC PU (equivalent to 33.33 mg, Ananas comosus — Stem)
A proteolytic enzyme complex derived from pineapple stem, studied for anti-inflammatory and tissue-support properties. Paired with papain to provide complementary enzymatic anti-inflammatory activity relevant to pelvic and prostate tissue.
Medicinal ingredients and quantities as licensed by Health Canada under NPN 80147704. Full ingredient list, exact quantities, and non-medicinal ingredients are printed on the product label and Health Canada licensing documentation. This page describes formulation rationale, not individual clinical claims for Pro-UROL itself.
For healthcare providers
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