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  4. NDC Product Code: 10956-674 Double Tussin Intense Cough Reliever DM

NDC 10956-674 Double Tussin Intense Cough Reliever DM

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 10956-674?
  5. Double Tussin Intense Cough Reliever DM Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
10956-674
Proprietary Name:
Double Tussin Intense Cough Reliever DM
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Reese Pharmaceutical Co
Labeler Code:
10956
Product Label ID:
067210f8-03bc-415c-9ec5-cdad04bfb07d
Start Marketing Date: [9]
08-02-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
Flavor(s):
CHERRY (C73375)

Product Packages

NDC Code 10956-674-01

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 120 mL in 1 BOTTLE, PLASTIC (10956-674-04)

NDC Code 10956-674-08

Package Description: 240 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 10956-674?

The NDC code 10956-674 is assigned by the FDA to the product Double Tussin Intense Cough Reliever DM which is product labeled by Reese Pharmaceutical Co. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 10956-674-01 1 bottle, plastic in 1 carton / 120 ml in 1 bottle, plastic (10956-674-04), 10956-674-08 240 ml in 1 bottle, plastic . 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 Double Tussin Intense Cough Reliever DM?

Uses. temporarily relieves cough due to minor throat and bronchial irritation as may occur with a common cold • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus • helps make coughs more productive

Which are Double Tussin Intense Cough Reliever DM UNII Codes?

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

Which are Double Tussin Intense Cough Reliever DM 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 Double Tussin Intense Cough Reliever DM?

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: 1117394 - dextromethorphan HBr 20 MG / guaiFENesin 300 MG in 5 mL Oral Solution
  • RxCUI: 1117394 - dextromethorphan hydrobromide 4 MG/ML / guaifenesin 60 MG/ML Oral Solution
  • RxCUI: 1117394 - dextromethorphan hydrobromide 20 MG / guaifenesin 300 MG per 5 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".