V-Fresh Restore Gel

V-Fresh Restore Gel is an FDA-registered drug product whose active ingredient is SOPHORA ALOPECUROIDES L. It is labelled by Shenzhen Xixi Beauty Industry Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87899-001, application 505G(a)(3), label effective 20260728. 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 SOPHORA ALOPECUROIDES L are most often described in connection with: helps moisturize, maintain vaginal, provide long-lasting, comfort supports, intimate microbiome. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Helps moisturize and maintain vaginal dryness Helps soothe and provide long-lasting comfort Supports intimate microbiome balance Helps maintain a healthy vaginal environment

Remove one tube from the package. Gently insert one tube into the vagina at bedtime. Use once daily or as recommended by a health professional. Discard the tube after use.

For external and vaginal use only.

What is V-Fresh Restore Gel used for?
Helps moisturize and maintain vaginal dryness Helps soothe and provide long-lasting comfort Supports intimate microbiome balance Helps maintain a healthy vaginal environment

Who makes V-Fresh Restore Gel?
Shenzhen Xixi Beauty Industry Co., Ltd. is the labeler of record for V-Fresh Restore Gel.

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

Is V-Fresh Restore Gel 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-Fresh Restore Gel 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.