YOBISIN

Manufacturer
Lydia Co., Ltd. | I World Pharmaceutical Co., Ltd.
Effective date
2023-12-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:04:44

Label at a glance#

ProductYOBISIN
Active ingredientRHUBARB, REHMANNIA GLUTINOSA ROOT, ANGELICA GIGAS ROOT, AKEBIA STEM, SCUTELLARIA BAICALENSIS ROOT, LICORICE, ALISMA PLANTAGO-AQUATICA ROOT, FORSYTHIA SUSPENSA FRUIT, PLANTAGO SEED, GINGER, CHINESE CINNAMON
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

rehmannia root, angelica gigas root, akebia stem, scutellaria root, alisma rhizome, plantago seed, licorice, gardenia fruit, gentian root and rhizome, cinnamomum cassia presl, raw ginger, rhubarb, ephdra heab, forsythia fruit

INACTIVE INGREDIENT SECTION

magnesium stearate, corn starch, polyethylene glycol 6000, hypromellose 2910

OTC - PURPOSE SECTION

bladder qatar, urethritis, kidney disease, nephrotic syndrome, edema

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

adults: 3~6 tablets twice a day

7 to 14 years old: 2-3 tablets twice a day

WARNINGS SECTION

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

DOSAGE & ADMINISTRATION SECTION

for oral use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GINGER Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
RHUBARB Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72988-0012-12023-12-16C16284748780-1ba0f9c33-309f-a910-e053-dadaa90a0b85Drug Facts
72988-0012-12021-01-29C16284748780-1ba0f9c33-309f-a910-e053-dadaa90a0b85Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72988-0012-1YOBISIN20 in 1 PACKAGETABLET203

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72988-0012YOBISIN (REHMANNIA ROOT, ANGELICA GIGAS ROOT) TABLET [LYDIA CO., LTD.]3Current NDC, Legacy NDC, 1 package rows20231217_873ef769-6051-4914-e053-2a95a90a9edb.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72988-001272988-0012-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
YOBISINREHMANNIA ROOT, ANGELICA GIGAS ROOTLydia Co., Ltd.873ef769-6051-4914-e053-2a95a90a9edb2023-12-16WarningsExact identifier
ndc (package): 72988-0012-1
ndc (product): 72988-0012
ndc11 (package): 72988001201
spl id: 0ca8ac22-aaac-9d25-e063-6294a90a4541
spl set id: 873ef769-6051-4914-e053-2a95a90a9edb

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.