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  4. NDC Product Code: 58066-8012 Four Seasons Flu Relief

NDC 58066-8012 Four Seasons Flu Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 58066-8012?
  4. Four Seasons Flu Relief 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:
58066-8012
Proprietary Name:
Four Seasons Flu Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Beaumont Bio Med
Labeler Code:
58066
Product Label ID:
9b5afd78-28be-4328-8f62-5787c682f86f
Start Marketing Date: [9]
01-08-2015
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 58066-8012-7

Package Description: 59.2 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 58066-8012?

The NDC code 58066-8012 is assigned by the FDA to the product Four Seasons Flu Relief which is product labeled by Beaumont Bio Med. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58066-8012-7 59.2 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 Four Seasons Flu Relief?

Indications: For temporary relief of flu-like symptoms: • Fever • Fatigue • Nausea • Cough • Runny nose • Congestion • Sore throat • Diarrhea •HeadacheUse according to label indications and/or standard homeopathic indications.

Which are Four Seasons Flu Relief UNII Codes?

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

Which are Four Seasons Flu Relief 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".