1. Home
  2. Labeler Index
  3. King Bio Inc
  4. NDC Product Code: 57955-3401 Fresh Thyme Flu Relief

NDC 57955-3401 Fresh Thyme Flu Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57955-3401?
  4. Fresh Thyme 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:
57955-3401
Proprietary Name:
Fresh Thyme Flu Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
King Bio Inc
Labeler Code:
57955
Product Label ID:
9956d317-2403-4589-a7ca-852ade3be2b8
Start Marketing Date: [9]
04-11-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 57955-3401-0

Package Description: 12 TUBE in 1 CARTON / 1 g in 1 TUBE

Product Details

What is NDC 57955-3401?

The NDC code 57955-3401 is assigned by the FDA to the product Fresh Thyme Flu Relief which is product labeled by King Bio Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 57955-3401-0 12 tube in 1 carton / 1 g in 1 tube. 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 Fresh Thyme Flu Relief?

​Adults and children 2 years of age and older: ​Dissolve entire contents of one tube in the mouth every 6 hours, up to 3 times per day.​For children yunger than age 2: ​Ask a doctor.

Which are Fresh Thyme Flu Relief UNII Codes?

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

  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (Active Moiety)

Which are Fresh Thyme 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:

* 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".