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  4. NDC Product Code: 43913-407 G-xpect Pse

NDC 43913-407 G-xpect Pse

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 43913-407?
  5. G-xpect Pse 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:
43913-407
Proprietary Name:
G-xpect Pse
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mclaren Medical
Labeler Code:
43913
Product Label ID:
19ca6998-8419-4da1-bd6f-7f4fd7477e47
Start Marketing Date: [9]
02-11-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
GRAPE (C73391)

Product Packages

NDC Code 43913-407-16

Package Description: 473 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 43913-407?

The NDC code 43913-407 is assigned by the FDA to the product G-xpect Pse which is product labeled by Mclaren Medical. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43913-407-16 473 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 G-xpect Pse?

For the temporary relief of nasal congestion due to the common cold, hay fever or other upper respiratory allergies (allergic rhinitis).Helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive.Temporarily controls cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants.Temporarily helps you cough less.

Which are G-xpect Pse UNII Codes?

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

Which are G-xpect Pse 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 G-xpect Pse?

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: 1421983 - dextromethorphan HBr 10 MG / guaiFENesin 200 MG / pseudoephedrine HCl 30 MG in 5 mL Oral Solution
  • RxCUI: 1421983 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 40 MG/ML / pseudoephedrine hydrochloride 6 MG/ML Oral Solution
  • RxCUI: 1421983 - dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / pseudoephedrine hydrochloride 30 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".