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  4. NDC Product Code: 59779-967 Tussin Dmmaximum Strength

NDC 59779-967 Tussin Dmmaximum Strength

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 59779-967?
  5. Tussin Dmmaximum Strength 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:
59779-967
Proprietary Name:
Tussin Dmmaximum Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cvs Pharmacy
Labeler Code:
59779
Product Label ID:
9bffd874-313f-4fbb-a196-b76bd7160f92
Start Marketing Date: [9]
07-01-2009
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)

Code Structure Chart

Product Details

What is NDC 59779-967?

The NDC code 59779-967 is assigned by the FDA to the product Tussin Dmmaximum Strength which is product labeled by Cvs Pharmacy. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 59779-967-03 1 bottle in 1 carton / 118 ml in 1 bottle, 59779-967-04 1 bottle in 1 carton / 237 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 Dmmaximum Strength?

Shake well before usingdo not take more than 6 doses in any 24-hour periodonly use the measuring cup that is included with this product for accurate dosingAgeDoseadults and children 12 years and over2 tsp (10ml) every 4 hourschildren under 12 yearsdo not use

Which are Tussin Dmmaximum Strength UNII Codes?

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

Which are Tussin Dmmaximum Strength 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 Dmmaximum Strength?

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: 1046631 - dextromethorphan HBr 20 MG / guaiFENesin 400 MG in 10 mL Oral Solution
  • RxCUI: 1046631 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 40 MG/ML Oral Solution
  • RxCUI: 1046631 - dextromethorphan HBr 10 MG / guaifenesin 200 MG per 5 ML Oral Solution
  • RxCUI: 1046631 - dextromethorphan HBr 20 MG / guaifenesin 400 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".