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  4. NDC Product Code: 43857-0194 Thymus

NDC 43857-0194 Thymus

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43857-0194?
  4. Thymus 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:
43857-0194
Proprietary Name:
Thymus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bioactive Nutrional, Inc.
Labeler Code:
43857
Product Label ID:
efde66a6-0571-41b5-b854-58a89551173b
Start Marketing Date: [9]
08-09-2013
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 43857-0194-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 43857-0194?

The NDC code 43857-0194 is assigned by the FDA to the product Thymus which is product labeled by Bioactive Nutrional, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43857-0194-1 30 ml in 1 bottle, spray . 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 Thymus?

Regulation and stimulation of the Thymus Gland. For temporary relief of symptoms due to lowered immune response, viral infections, or influenza. Regulation and stimulation of the Thymus Gland. For temporary relief of symptoms due to lowered immune response, viral infections, or influenza.

Which are Thymus UNII Codes?

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

Which are Thymus 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".