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  4. NDC Product Code: 58906-1001 Burzangmury Gold

NDC 58906-1001 Burzangmury Gold

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 58906-1001?
  4. Burzangmury Gold 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:
58906-1001
Proprietary Name:
Burzangmury Gold
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dae Deok Bio Inc
Labeler Code:
58906
Product Label ID:
d9719323-78c2-4b6b-a35b-436452a8a5ea
Start Marketing Date: [9]
08-01-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 58906-1001?

The NDC code 58906-1001 is assigned by the FDA to the product Burzangmury Gold which is product labeled by Dae Deok Bio Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58906-1001-1 500 ml in 1 bottle, plastic . 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 Burzangmury Gold?

After throughly wetting the hair and scalp with water and  putting a dollop of shampoo on the hair, massage your scalp for 2~3 minutes with foam and rinse away the shampoo. A person who have problem with hair or a person with long hair can have more effect by shampooing one more time

Which are Burzangmury Gold UNII Codes?

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

Which are Burzangmury Gold 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".