81651-0001 NDC - COZACO MAN (RED GINSENG)

Drug Information

Product NDC: 81651-0001

Proprietary Name: COZACO MAN

Non Proprietary Name: Red ginseng

Active Ingredient(s):
  • 21.19 1/1 PANAX GINSENG ROOT OIL


Administration Route(s): ORAL

Dosage Form(s): TABLET

Labeler Information

Labeler Name: Kone Bio Logics Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:3/10/2021

Package Information

No. Package Code Package Description Billing Unit
181651-0001-1100 TABLET in 1 BOTTLE (81651-0001-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC81651-0001The 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 NAMECOZACO MANThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMERed ginsengThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLETThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE3/10/2021This 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 NAMEKone Bio Logics Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEPANAX GINSENG ROOT OILAn 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 STRENGTH21.19 
ACTIVE INGRED UNIT1/1 

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