FDA.reportPublic FDA data

Yiganerjing Herbal

Manufacturer
TAIZHOU YOUPENG IMPORT AND EXPORT TRADING CO., LTD | JIANGXI YANGZHENG BIOLOGY AND TECHNOLOGY CO., LTD
Effective date
2018-02-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:54:27

Label at a glance#

ProductYiganerjing Herbal
Active ingredientTYPHONIUM GIGANTEUM WHOLE
Label structure6 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Purpose: 

Prevent bacteria growth

WARNINGS SECTION

Warning:

External use only. Not to take orally. Seek professional help if itch or redness occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children under 18 years old, please do not use.

DOSAGE & ADMINISTRATION SECTION

Instruction for use:

Apply a thin layer of the ointment to affected area, massage gently until absorbed completely.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Propanetriol,Cortex Dictamni,Gleditsia sinensis Linn,Rhizoma Smilacis Glabrae,Pseudolarix amabilis Rehd,Sophora Flav,Stemcna Tuberosa.Lour,Louresvens,Cnidium monnieri(L.)Cuss,Latin Tile,Pheiiodendron amurense Rupr,Rotuda Thunb,Mentholum,Chlorhexidine acetate,Stearic acid, Glycerol monostearate,Albolene,Atolin, Sorbitan Stearate,Ethylparaben,Polyoxyethylene 20 Sorbitan Monostearate,Propanetriol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71939-001-012020-01-31C16284748780-19d75b9d0-9520-f424-e053-dadaa90a57ceb39d1853-c058-4f6a-afd4-a8ddc4f1cccd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71939-001-01Yiganerjing Herbal15 g in 1 TUBECREAM151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71939-001YIGANERJING HERBAL (TYPHONIUM GIGANTEUM WHOLE) CREAM [TAIZHOU YOUPENG IMPORT AND EXPORT TRADING CO., LTD]1Legacy NDC, 1 package rows20180210_b39d1853-c058-4f6a-afd4-a8ddc4f1cccd.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71939-00171939-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLEDITSIA SINENSIS FRUITA6W0J6UO7QIACT
PSEUDOLARIX AMABILIS WHOLEG2TMJ38TAUIACT
SOPHORA FLAVESCENS WHOLEX8KX602M5LIACT
CNIDIUM MONNIERI FRUITV1IA3S3CUSIACT
MENTHOLL7T10EIP3AIACT
CHLORHEXIDINE ACETATE5908ZUF22YIACT
STEARIC ACID4ELV7Z65APIACT
ETHYLPARABEN14255EXE39IACT
TYPHONIUM GIGANTEUM WHOLEC61Y66MY4HACTIM

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
64cb887a-9529-0699-e053-2991aa0a047fb39d1853-c058-4f6a-afd4-a8ddc4f1cccd2018-02-09WarningsExact identifier
spl id: 64cb887a-9529-0699-e053-2991aa0a047f
spl set id: b39d1853-c058-4f6a-afd4-a8ddc4f1cccd

Reported adverse events (FAERS/openFDA)#

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