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  4. NDC Product Code: 67510-0506 Tussin Cf

NDC 67510-0506 Tussin Cf

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 67510-0506?
  4. Tussin Cf Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
67510-0506
Proprietary Name:
Tussin Cf
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kareway Product, Inc.
Labeler Code:
67510
Product Label ID:
5f8dffc8-ffee-4ca9-b37d-40ccad2ba86a
Start Marketing Date: [9]
08-26-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 67510-0506?

The NDC code 67510-0506 is assigned by the FDA to the product Tussin Cf which is product labeled by Kareway Product, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 67510-0506-4 1 bottle in 1 box / 120 ml in 1 bottle. 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 Tussin Cf?

Do not take more than 6 doses in any 24-hour periodAgeDoseadults and children 12 years and over2 tsp every 4 hourschildren 6 years to under 12 years1 tsp every 4 hourschildren 2 years to under 6 years1/2 tsp every 4 hourschildren under 2 yearsask a doctor

Which are Tussin Cf UNII Codes?

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

Which are Tussin Cf 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:

What is the NDC to RxNorm Crosswalk for Tussin Cf?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1044949 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG / phenylephrine HCl 10 MG in 10 mL Oral Solution
  • RxCUI: 1044949 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 1 MG/ML Oral Solution
  • RxCUI: 1044949 - dextromethorphan HBr 10 MG / guaifenesin 100 MG / phenylephrine HCl 5 MG per 5 ML Oral Solution
  • RxCUI: 1044949 - dextromethorphan HBr 20 MG / guaifenesin 200 MG / phenylephrine HCl 10 MG per 10 ML Oral Solution

* 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".