V-Bella

V-Bella is an FDA-registered drug product whose active ingredient is BORIC ACID. It is labelled by U.S. PHARMACEUTICAL CORPORATION taken by vaginal and marketed as a human otc drug product. Identifiers on file: NDC 52747-155, label effective 20221117. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing BORIC ACID are most often described in connection with: relieves symptoms, urinary infections, rebalances vaginal, restores normal, health helps, burning itching, odor due. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses treats and relieves symptoms of vaginal and urinary infections. rebalances vaginal pH and restores normal vaginal health. helps relieve symptoms of external and internal vaginal burning, itching, irritation and dryness. helps reduce vaginal odor due to vaginal infections.

Directions before using this product, read all consumer information provided on carton and insert, Adults and children 12 years of age and over: place vaginal capsule suppository in applicator and gently insert into the vagina. for acute infection, use one (1) capsule suppository a day for three (3) days for chronic infection, use an additional package of three (3) vaginal capsule suppositories throw applicator away after each use Children under 12 years of age: ask a doctor

Warnings For vaginal use only

What is V-Bella used for?
Uses treats and relieves symptoms of vaginal and urinary infections. rebalances vaginal pH and restores normal vaginal health. helps relieve symptoms of external and internal vaginal burning, itching, irritation and dryness. helps reduce vaginal odor due to vaginal infections.

Who makes V-Bella?
U.S. PHARMACEUTICAL CORPORATION is the labeler of record for V-Bella.

What form does V-Bella come in?
administered by vaginal. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is V-Bella prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has V-Bella been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.