YOBISIN
YOBISIN is an FDA drug label for the active ingredient REHMANNIA ROOT, ANGELICA GIGAS ROOT manufactured by Lydia Co., Ltd. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231216.
- Generic name
- REHMANNIA ROOT, ANGELICA GIGAS ROOT
- Manufacturer
- Lydia Co., Ltd.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 72988-0012
- Application
- N/A
- Label effective
- 20231216
About this product
YOBISIN is an FDA-registered drug product whose active ingredient is REHMANNIA ROOT, ANGELICA GIGAS ROOT. It is labelled by Lydia Co., Ltd. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 72988-0012, 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.
What it is used for
Across FDA labelling, products containing REHMANNIA ROOT, ANGELICA GIGAS ROOT are most often described in connection with: tablets twice, day years. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
adults: 3~6 tablets twice a day 7 to 14 years old: 2-3 tablets twice a day
Dosage & Administration
for oral use only
Warnings
do not take this medicine if you have following symptoms children under 6 years old women who are likely to be pregnant or pregnant breastfeeding
Frequently asked questions
What is YOBISIN used for?
adults: 3~6 tablets twice a day 7 to 14 years old: 2-3 tablets twice a day
Who makes YOBISIN?
Lydia Co., Ltd. is the labeler of record for YOBISIN.
What form does YOBISIN 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 YOBISIN 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 YOBISIN 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.