72850-0003 NDC - GORYEODYO GOYAK (AMPELOPSIS RADIX , ANGELICA DAHURICA ROOT)

Drug Information

Product NDC: 72850-0003

Proprietary Name: Goryeodyo Goyak

Non Proprietary Name: Ampelopsis Radix , Angelica Dahurica Root

Active Ingredient(s):
  • 3.75 g/100g AMPELOPSIS JAPONICA TUBER;
  • 1.88 g/100g ANGELICA DAHURICA ROOT;
  • 1.88 g/100g ANGELICA GIGAS ROOT OIL;
  • 1.88 g/100g APRICOT KERNEL OIL;
  • 1.88 g/100g ASTRAGALUS PROPINQUUS ROOT;
  • 1.88 g/100g BLETILLA STRIATA TUBER;
  • 1.88 g/100g CINNAMON BARK OIL;
  • .1 g/100g CITRUS AURANTIUM FRUIT RIND;
  • 1.88 g/100g FRANKINCENSE;
  • 25 g/100g LEAD TETROXIDE;
  • 1.88 g/100g MOMORDICA COCHINCHINENSIS SEED;
  • 1.88 g/100g MYRRH;
  • 1.88 g/100g PAEONIA LACTIFLORA ROOT;
  • 1.88 g/100g PHELLODENDRON CHINENSIS BARK;
  • 1.88 g/100g REHMANNIA GLUTINOSA ROOT;
  • 7.5 g/100g RHUBARB;
  • 1.8 g/100g SCROPHULARIA BUERGERIANA ROOT;
  • 7.5 g/100g SCUTELLARIA BAICALENSIS ROOT;
  • .1 g/100g SULFUR;
  • 3.75 g/100g YELLOW WAX


Administration Route(s): TOPICAL

Dosage Form(s): OINTMENT

Pharmacy Class(es):
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Increased Histamine Release [PE];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Plant Proteins [CS]

Labeler Information

Labeler Name: Chunwoo Pharmaceutical Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:3/19/2019

Package Information

No. Package Code Package Description Billing Unit
172850-0003-14 g in 1 BOX (72850-0003-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC72850-0003The 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 NAMEGoryeodyo GoyakThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAmpelopsis Radix , Angelica Dahurica RootThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEOINTMENTThe 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 DATE3/19/2019This 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 NAMEChunwoo Pharmaceutical Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAMPELOPSIS JAPONICA TUBER; ANGELICA DAHURICA ROOT; ANGELICA GIGAS ROOT OIL; APRICOT KERNEL OIL; ASTRAGALUS PROPINQUUS ROOT; BLETILLA STRIATA TUBER; CINNAMON BARK OIL; CITRUS AURANTIUM FRUIT RIND; FRANKINCENSE; LEAD TETROXIDE; MOMORDICA COCHINCHINENSIS SEED; MYRRH; PAEONIA LACTIFLORA ROOT; PHELLODENDRON CHINENSIS BARK; REHMANNIA GLUTINOSA ROOT; RHUBARB; SCROPHULARIA BUERGERIANA ROOT; SCUTELLARIA BAICALENSIS ROOT; SULFUR; YELLOW WAXAn 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 STRENGTH3.75; 1.88; 1.88; 1.88; 1.88; 1.88; 1.88; .1; 1.88; 25; 1.88; 1.88; 1.88; 1.88; 1.88; 7.5; 1.8; 7.5; .1; 3.75 
ACTIVE INGRED UNITg/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g; g/100g 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] 

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