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  4. NDC Product Code: 50653-2001 Bonogen Plus Hair Care Shampoo

NDC 50653-2001 Bonogen Plus Hair Care Shampoo

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50653-2001?
  4. Active Ingredients UNII Codes
  5. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50653-2001
Proprietary Name:
Bonogen Plus Hair Care Shampoo
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bonogen Co., Ltd
Labeler Code:
50653
Product Label ID:
db08ca91-b9f9-4a2e-b8ab-b7a51e70010d
Start Marketing Date: [9]
04-09-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 50653-2001?

The NDC code 50653-2001 is assigned by the FDA to the product Bonogen Plus Hair Care Shampoo which is product labeled by Bonogen Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50653-2001-1 100 g in 1 bottle . 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.

Which are Bonogen Plus Hair Care Shampoo UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Bonogen Plus Hair Care Shampoo?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1044982 - biotin 0.06 % / nadide 0.3 % / panthenol 0.6 % / zinc pyrithione 2.1 % Medicated Shampoo
  • RxCUI: 1044982 - biotin 0.6 MG/ML / nicotinamide adenine dinucleotide (NAD) 3 MG/ML / panthenol 6 MG/ML / zinc pyrithione 21 MG/ML Medicated Shampoo

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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".