Doctor brochure
For women prone to recurrent UTI and BV. When to recommend UroRAIN, suggested capsules per day for each indication, and the formula at a glance.
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The information on this page is intended for registered healthcare professionals in Singapore. It includes clinical study summaries that are not intended for the general public.
Fact sheets, evidence summaries and product documentation for clinics and pharmacies. UroRAIN combines D-Mannose, cranberry PACs and a 7-strain Lactobacillus complex with FOS, made in Singapore.

Two-page A4 sheets, ready to print or share with your team.
For women prone to recurrent UTI and BV. When to recommend UroRAIN, suggested capsules per day for each indication, and the formula at a glance.
Download PDFThe three mechanisms, formula per serving, and the evidence for cranberry PACs, D-Mannose and L. crispatus.
Download PDFThe seven strains and the evidence on oral lactobacilli for vaginal flora, bacterial vaginosis and candidiasis.
Download PDFBinds E. coli type 1 fimbriae so bacteria are cleared with urine.
A-type proanthocyanidins inhibit adhesion of P-fimbriated E. coli to the urothelium.
15 billion CFU including L. crispatus, supporting protective flora and an acidic vaginal pH.
Published studies on the individual ingredients, at the doses and routes studied.
In women with recurrent UTI, cranberry products probably reduce symptomatic, culture-verified UTI (RR 0.74, 95% CI 0.55–0.99).
2 g/day for 6 months: recurrence 14.6% vs 60.8% with no prophylaxis, comparable to nitrofurantoin 50 mg (20.4%). UroRAIN provides 1 g/day.
Intravaginal L. crispatus: recurrent UTI 15% vs 27% on placebo (RR 0.5, 95% CI 0.2–1.2). UroRAIN delivers L. crispatus orally.
Oral L. rhamnosus GR-1 + L. fermentum RC-14 for 60 days restored a lactobacilli-dominant flora in 37% vs 13% on placebo.
Oral L. rhamnosus GR-1 + L. reuteri RC-14 for 6 weeks: balanced microbiota in 61.5% vs 26.9% on placebo.
As an adjunct to antifungals, probiotics increased short-term clinical cure (RR 1.14) and reduced one-month relapse (RR 0.34). Evidence quality low.
Certificate of analysis, GMP certificate and FDA facility registration are available on request for each batch.
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