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  4. NDC Product Code: 72850-0006 Band Leemyungnae Goyak

NDC 72850-0006 Band Leemyungnae Goyak

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72850-0006?
  4. Band Leemyungnae Goyak Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72850-0006
Proprietary Name:
Band Leemyungnae Goyak
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Chunwoo Pharmaceutical Co., Ltd.
Labeler Code:
72850
Product Label ID:
9c4edf55-d91c-29ff-e053-2a95a90a2a10
Start Marketing Date: [9]
03-22-2019
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72850-0006-1

Package Description: 3 g in 1 BOX

Product Details

What is NDC 72850-0006?

The NDC code 72850-0006 is assigned by the FDA to the product Band Leemyungnae Goyak which is product labeled by Chunwoo Pharmaceutical Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72850-0006-1 3 g 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 Band Leemyungnae Goyak?

■ Wash your hands and clean affected area■ before a boil or a pus is festering, attach the plaster only to cover the affected area.■ when a boil or a pus festering, insert an uprooting ointment into the area and attach the plaster on it.■ Change to a new plaster after a day or two while symptom persists.

Which are Band Leemyungnae Goyak UNII Codes?

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

Which are Band Leemyungnae Goyak 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".