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  4. NDC Product Code: 40032-050 Polyethylene Glycol-3350, Sodium Chloride, Potassium Chloride And Sodium Bicarbonate

NDC 40032-050 Polyethylene Glycol-3350, Sodium Chloride, Potassium Chloride And Sodium Bicarbonate

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 40032-050?
  5. Polyethylene Glycol-3350, Sodium Chloride, Potassium Chloride And Sodium Bicarbonate 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:
40032-050
Proprietary Name:
Polyethylene Glycol-3350, Sodium Chloride, Potassium Chloride And Sodium Bicarbonate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Novel Laboratories, Inc.
Labeler Code:
40032
Product Label ID:
444c83ae-ac3a-467c-be05-e2bcbfbaaba1
Start Marketing Date: [9]
05-28-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
LEMON (C73396)

Product Packages

NDC Code 40032-050-19

Package Description: 438.4 g in 1 BOTTLE

Product Details

What is NDC 40032-050?

The NDC code 40032-050 is assigned by the FDA to the product Polyethylene Glycol-3350, Sodium Chloride, Potassium Chloride And Sodium Bicarbonate which is product labeled by Novel Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 40032-050-19 438.4 g 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 Polyethylene Glycol-3350, Sodium Chloride, Potassium Chloride And Sodium Bicarbonate?

PEG-3350, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM BICARBONATE for Oral Solution is indicated for bowel cleansing prior to colonoscopy.

Which are Polyethylene Glycol-3350, Sodium Chloride, Potassium Chloride And Sodium Bicarbonate UNII Codes?

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

Which are Polyethylene Glycol-3350, Sodium Chloride, Potassium Chloride And Sodium Bicarbonate 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 Polyethylene Glycol-3350, Sodium Chloride, Potassium Chloride And Sodium Bicarbonate?

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: 801054 - PEG-3350 420 GM / sodium chloride 11.2 GM / sodium bicarbonate 5.72 GM / potassium chloride 1.48 GM Powder for Oral Solution
  • RxCUI: 801054 - polyethylene glycol 3350 420000 MG / potassium chloride 1480 MG / sodium bicarbonate 5720 MG / sodium chloride 11200 MG Powder for Oral Solution
  • RxCUI: 801054 - PEG 3350 420 GM / potassium chloride 1.48 GM / sodium bicarbonate 5.72 GM / sodium chloride 11.2 GM per 4 L Powder for Oral Solution
  • RxCUI: 801054 - PEG-3350 420 GM / KCl 1.48 GM / NaCl 11.2 GM / NaHCO3 5.72 GM Powder for 4 L Oral Solution
  • RxCUI: 801054 - POLYETHYLENE GLYCOL 3350 420000 MG / K+ Chloride 1480 MG / NaHCO3 5720 MG / NaCl 11200 MG Powder for 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".