NDC 82877-002 Nekvnro Varicose Veins Patch

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
82877-002
Proprietary Name:
Nekvnro Varicose Veins Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
82877
Start Marketing Date: [9]
09-05-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 82877-002?

The NDC code 82877-002 is assigned by the FDA to the product Nekvnro Varicose Veins Patch which is product labeled by Shenzhen Boceda New Technology Co., Ltd.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 82877-002-01 7 patch in 1 box , 82877-002-02 15 patch in 1 box , 82877-002-03 50 patch in 1 box , 82877-002-04 100 patch in 1 box . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Nekvnro Varicose Veins Patch?

Place Enough Product On Hands To Cover All Surfaces. Massage To Absorb Supervise Children Under 6 Years Of Age When Using This Product To Avoid Swallowing. Other Information [Storage And Handling Section]edit Store Between 15-30c (59-86f) Avoid Freezing And Excessive Heat Above 40c (104f)

Which are Nekvnro Varicose Veins Patch UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Nekvnro Varicose Veins Patch Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".