82877-002 NDC - NEKVNRO VARICOSE VEINS PATCH

Drug Information

Product NDC: 82877-002

Proprietary Name: Nekvnro Varicose Veins Patch

Non Proprietary Name: Nekvnro Varicose Veins Patch

Active Ingredient(s):
  • .5 g/1001 BORNEOL;
  • .3 g/1001 CAPSAICIN;
  • .8 g/1001 MENTHOL


Administration Route(s): TOPICAL

Dosage Form(s): PATCH

Labeler Information

Labeler Name: Shenzhen Boceda New Technology Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/5/2022

Package Information

No. Package Code Package Description Billing Unit
182877-002-017 PATCH in 1 BOX (82877-002-01)
282877-002-0215 PATCH in 1 BOX (82877-002-02)
382877-002-0350 PATCH in 1 BOX (82877-002-03)
482877-002-04100 PATCH in 1 BOX (82877-002-04)

NDC Record

Field Name Field Value Definition
PRODUCT NDC82877-002The 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 NAMENekvnro Varicose Veins PatchThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMENekvnro Varicose Veins PatchThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPATCHThe 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 DATE9/5/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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 NAMEShenzhen Boceda New Technology Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEBORNEOL; CAPSAICIN; MENTHOLAn 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.5; .3; .8 
ACTIVE INGRED UNITg/1001; g/1001; g/1001 

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

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