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  4. NDC Product Code: 45984-0002 Neobryxol Forte

NDC 45984-0002 Neobryxol Forte

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 45984-0002?
  4. Neobryxol Forte 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:
45984-0002
Proprietary Name:
Neobryxol Forte
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bryomed Inc.
Labeler Code:
45984
Product Label ID:
f77e0d17-44de-4ac0-84a4-dcb3cb83cd33
Start Marketing Date: [9]
04-04-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 45984-0002?

The NDC code 45984-0002 is assigned by the FDA to the product Neobryxol Forte 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 45984-0002-1 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 Neobryxol Forte?

Indication: Maintains the system under the stress of malignancy regardless of location. Targets tissues that tend to be more susceptible to cancer, neuralgias and dropsy of extremities, yellowed skin, headache, physical weakness and rheumatic pains.Based on the homeopathic Materia  Medicas.Reference image forte.jpg

Which are Neobryxol Forte UNII Codes?

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

Which are Neobryxol Forte 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".