71939-003 NDC - YIGANERJING SUIFURSOAP

Drug Information

Product NDC: 71939-003

Proprietary Name: YIGANERJING SuifurSoap

Non Proprietary Name: YIGANERJING SuifurSoap

Active Ingredient(s):
  • .0672 g/84g EDETIC ACID;
  • .84 g/84g SULFUR;
  • .168 g/84g TITANIUM DIOXIDE


Administration Route(s): TOPICAL

Dosage Form(s): SOAP

Pharmacy Class(es):
  • Anti-coagulant [EPC];
  • Calcium Chelating Activity [MoA];
  • Decreased Coagulation Factor Activity [PE];
  • Lead Chelating Activity [MoA];
  • Lead Chelator [EPC]

Labeler Information

Labeler Name: TAIZHOU YOUPENG IMPORT AND EXPORT TRADING CO.,LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:6/22/2020

Package Information

No. Package Code Package Description Billing Unit
171939-003-0184 g in 1 BOX (71939-003-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71939-003The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEYIGANERJING SuifurSoapThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEYIGANERJING SuifurSoapThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOAPThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE6/22/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMETAIZHOU YOUPENG IMPORT AND EXPORT TRADING CO.,LTD.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEEDETIC ACID; SULFUR; TITANIUM DIOXIDEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH.0672; .84; .168 
ACTIVE INGRED UNITg/84g; g/84g; g/84g 
PHARM CLASSESAnti-coagulant [EPC], Calcium Chelating Activity [MoA], Decreased Coagulation Factor Activity [PE], Lead Chelating Activity [MoA], Lead Chelator [EPC] 

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This page was last updated on: 2/1/2023