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  4. NDC Product Code: 59240-004 Keptrils

NDC 59240-004 Keptrils

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 59240-004?
  5. Keptrils 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:
59240-004
Proprietary Name:
Keptrils
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Magverz Inc
Labeler Code:
59240
Product Label ID:
f162ff52-19e5-43d8-a275-ed0c0b5724cd
Start Marketing Date: [9]
09-03-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
ROUND (C48348)
Size(s):
24 MM
Score:
1

Product Packages

NDC Code 59240-004-01

Package Description: 24 LOZENGE in 1 PACKAGE

Product Details

What is NDC 59240-004?

The NDC code 59240-004 is assigned by the FDA to the product Keptrils which is product labeled by Magverz Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59240-004-01 24 lozenge in 1 package . 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 Keptrils?

Adults and childrens 6 years older: allow lozene to dissolve slowly in the mouth; may be repeated every two hours as nedded or as directed by doctor or dentist .Childrens under 6 years of age; do not use.

Which are Keptrils UNII Codes?

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

Which are Keptrils 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 Keptrils?

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 code indicates a single concept unique identifier (RXCUI) is associated with this product:

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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".