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  4. NDC Product Code: 57955-6145 Childrens Cough Relief

NDC 57955-6145 Childrens Cough Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57955-6145?
  4. Childrens Cough 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:
57955-6145
Proprietary Name:
Childrens Cough Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
King Bio Inc.
Labeler Code:
57955
Product Label ID:
1e651ce1-f0fd-43dc-91df-05879272d75a
Start Marketing Date: [9]
12-01-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 57955-6145?

The NDC code 57955-6145 is assigned by the FDA to the product Childrens Cough 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 57955-6145-2 59 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 Childrens Cough Relief?

Uses for temporary relief of minor cough symptoms from the common cold or inhaled irritants:dry or hoarse coughtickling cough cough from mucus drainage or throat irritationNote: A persistent cough may be a sign of a serious condition. If cough is accompanied by fever, rash, persistent headache or breathing difficulties, consult a physician.Reference image cough.jpg

Which are Childrens Cough Relief UNII Codes?

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

Which are Childrens Cough 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".