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  4. NDC Product Code: 51445-101 Therabiogen Cold And Flu Relief Nasal

NDC 51445-101 Therabiogen Cold And Flu Relief Nasal

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51445-101?
  4. Therabiogen Cold And Flu Relief Nasal 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:
51445-101
Proprietary Name:
Therabiogen Cold And Flu Relief Nasal
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Therabiogen
Labeler Code:
51445
Product Label ID:
17704cc5-96f1-4d10-b5f6-252c6491db49
Start Marketing Date: [9]
09-29-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 51445-101?

The NDC code 51445-101 is assigned by the FDA to the product Therabiogen Cold And Flu Relief Nasal which is product labeled by Therabiogen. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51445-101-15 1 bottle, spray in 1 box / 15 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 Therabiogen Cold And Flu Relief Nasal?

UsesRelieves old and flu symptoms Provides relief from upper respiratory symptoms such as nasal and sinus congestion, runny nose, sore throat, sneezing and headacheAlso relieves fever, chills and body aches associated with the flu

Which are Therabiogen Cold And Flu Relief Nasal UNII Codes?

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

Which are Therabiogen Cold And Flu Relief Nasal 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".