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  4. NDC Product Code: 77130-0004 B100

NDC 77130-0004 B100

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 77130-0004?
  4. B100 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:
77130-0004
Proprietary Name:
B100
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sejin E&p Co., Ltd.
Labeler Code:
77130
Product Label ID:
a4a1c168-360f-2cfc-e053-2a95a90a8c32
Start Marketing Date: [9]
05-02-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 77130-0004-1

Package Description: 100 g in 1 PACKAGE

Product Details

What is NDC 77130-0004?

The NDC code 77130-0004 is assigned by the FDA to the product B100 which is product labeled by Sejin E&p Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 77130-0004-1 100 g in 1 package . 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 B100?

This product can not be eaten. And do not use it for other purposesAvoid using in places exposed to high temperatures and direct sunlight for prolonged periods of time.Put or Inserted in employee ID case, handbag, wallet, pocket or mask storage case.

Which are B100 UNII Codes?

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

Which are B100 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".