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  4. NDC Product Code: 59623-005 Cold And Flu Formula

NDC 59623-005 Cold And Flu Formula

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59623-005?
  4. Cold And Flu Formula 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:
59623-005
Proprietary Name:
Cold And Flu Formula
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Integrative Healing Institute, Llc
Labeler Code:
59623
Product Label ID:
ce1f9a0a-4192-469c-b0db-bd5f55126176
Start Marketing Date: [9]
11-04-2013
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 59623-005?

The NDC code 59623-005 is assigned by the FDA to the product Cold And Flu Formula which is product labeled by Integrative Healing Institute, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59623-005-02 59 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 Cold And Flu Formula?

Use:  This product is a Homeopathic Dilution, formulated to support the body's immunity for the relief of cold and flu symptoms.

Which are Cold And Flu Formula UNII Codes?

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

Which are Cold And Flu Formula 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".