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  4. NDC Product Code: 70005-044 Cough Suppressant And Expectorant Dm

NDC 70005-044 Cough Suppressant And Expectorant Dm

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 70005-044?
  5. Cough Suppressant And Expectorant 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:
70005-044
Proprietary Name:
Cough Suppressant And Expectorant Dm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
We Care Distributor Inc.
Labeler Code:
70005
Product Label ID:
2f8ed05f-7e52-4714-895a-912008d1b74f
Start Marketing Date: [9]
06-29-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
CHERRY (C73375 - CHERRY)

Code Structure Chart

Product Details

What is NDC 70005-044?

The NDC code 70005-044 is assigned by the FDA to the product Cough Suppressant And Expectorant Dm which is product labeled by We Care Distributor Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70005-044-01 1 bottle, plastic in 1 carton / 60 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 Cough Suppressant And Expectorant Dm?

Do not take more than 6 doses in a 24-hour periodRepeat dose every 4 hours while symptoms last          AGE                                     DOSEadults and children12 years of age and over               10 mL     children 6 years tounder 12 years of age                    5 mLchildren 2 years tounder 6 years of age                      2.5 mLchildren underunder 2 years of age                      ask a doctor

Which are Cough Suppressant And Expectorant Dm UNII Codes?

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

Which are Cough Suppressant And Expectorant 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 Cough Suppressant And Expectorant 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: 996520 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG in 10 mL Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 10 MG / guaifenesin 100 MG per 5 ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 15 MG / guaifenesin 150 MG per 7.5 ML Oral Solution
  • RxCUI: 996520 - dextromethorphan hydrobromide 20 MG / guaifenesin 200 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".