BAENOSIN

BAENOSIN is an FDA-registered drug product whose active ingredient is PLATYCODON ROOT, LICORICE, JUJUBE, PEONY ROOT. It is labelled by Lydia Co., Ltd. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 72988-0011, label effective 20231216. 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 PLATYCODON ROOT, LICORICE, JUJUBE, PEONY ROOT are most often described in connection with: adults take, capsules times. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

adults take 2 capsules 3 times a day before meals or between meals

for oral use only

do not take this medicine if you have following symptoms symptoms of headaches, chills, and fever other than local symptoms such as spasm (red with blood), swelling, and pain at the same time

What is BAENOSIN used for?
adults take 2 capsules 3 times a day before meals or between meals

Who makes BAENOSIN?
Lydia Co., Ltd. is the labeler of record for BAENOSIN.

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

Is BAENOSIN 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 BAENOSIN 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.