1. Home
  2. Labeler Index
  3. Bryomed Inc
  4. NDC Product Code: 45984-0001 Neobryxol Neb

NDC 45984-0001 Neobryxol Neb

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 45984-0001?
  4. Neobryxol Neb 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:
45984-0001
Proprietary Name:
Neobryxol Neb
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bryomed Inc
Labeler Code:
45984
Product Label ID:
5a783af4-c84e-44a6-b073-52fa1309b381
Start Marketing Date: [9]
01-04-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 45984-0001?

The NDC code 45984-0001 is assigned by the FDA to the product Neobryxol Neb which is product labeled by Bryomed Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 45984-0001-1 60 ml in 1 bottle, dropper . 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 Neobryxol Neb?

A natural aid in the treatment of chronic cough, chest pain, mucus congestion, bleeding of the lungs, shortness of breath, difficult respiration, hoarseness, hay fever, asthma, recurring pneumonia, mental or physical fatigue, during times of chronic disease or malignancy. Based on the homeopathic Materia Medicas.Reference image neb.jpg

Which are Neobryxol Neb UNII Codes?

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

Which are Neobryxol Neb 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:

* Please review the disclaimer below.

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".