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  4. NDC Product Code: 76509-200 Kids Cold

NDC 76509-200 Kids Cold

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76509-200?
  4. Kids Cold 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:
76509-200
Proprietary Name:
Kids Cold
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Natures Investment Holdings Pty Ltd Dba Maxrelief Usa
Labeler Code:
76509
Product Label ID:
f660e851-4832-4f40-8de9-a9a4733a19cf
Start Marketing Date: [9]
04-30-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 76509-200?

The NDC code 76509-200 is assigned by the FDA to the product Kids Cold which is product labeled by Natures Investment Holdings Pty Ltd Dba Maxrelief Usa. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76509-200-02 10 cello pack in 1 box / 1 lozenge in 1 cello pack (76509-200-01). 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 Kids Cold?

Indications for kids cough:For natural, temporary relief of pain and discomfort of Cough, Cold and Throat symptoms. Indications for kids cold:For natural, temporary relief of pain anddiscomfort of Cough, Cold and Throat symptoms.Indications for kids throat:For natural, temporary relief of pain and discomfort of Cough, Cold and Throat symptoms.

Which are Kids Cold UNII Codes?

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

Which are Kids Cold 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".