YSNORE

YSNORE is an FDA-registered drug product whose active ingredient is DIOSCOREA VILLOSA ROOT, GINGER. It is labelled by Y Snore taken by nasal and marketed as a human otc drug product. Identifiers on file: NDC 62587-219, label effective 20180109. 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 DIOSCOREA VILLOSA ROOT, GINGER are most often described in connection with: clinically proven, reduce stop, symptoms snoring. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Clinically proven to reduce or stop the symptoms of snoring.

Directions Use only as directed • Shake well before use. • With head upright 1 or 2 sprays at the base of each nostril prior to sleep. • Store at room temperature not to exceed 80° F. • For individual use only. • For best results daily use is required.

Warnings • Do not use on children under 12 years of age.

What is YSNORE used for?
Uses Clinically proven to reduce or stop the symptoms of snoring.

Who makes YSNORE?
Y Snore is the labeler of record for YSNORE.

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

Is YSNORE 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 YSNORE 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.