NDC 76509-150 Kids Cough

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
76509-150
Proprietary Name:
Kids Cough
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
Start Marketing Date: [9]
02-12-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 76509-150-01

Package Description: 10 LOZENGE in 1 BOX

NDC Code 76509-150-02

Package Description: 10 LOZENGE in 1 BOX

Product Details

What is NDC 76509-150?

The NDC code 76509-150 is assigned by the FDA to the product Kids Cough which is product labeled by Natures Investment Holdings Pty Ltd Dba Maxrelief Usa. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 76509-150-01 10 lozenge in 1 box , 76509-150-02 10 lozenge in 1 box . 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 Cough?

Indications for kids cough apple:For natural, temporary relief of coughand sore throat symptoms (hoarseness and dry cough). If coughing persists, consult a heathcare professional. Indications for kids cough orange:For natural, temporary relief of coughand sore throat symptoms (hoarseness anddry cough). If coughing persists,consult a healthcare professional.Indications for kids cough raspberry:For natural, temporary relief of coughand sore throat symptoms (hoarseness anddry cough). If coughing persists, consult a healthcare professional.

Which are Kids Cough UNII Codes?

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

Which are Kids Cough 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".