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  4. NDC Product Code: 54157-109 Upc 801803 00211 Megafresh Gel Fluoride Tooth

NDC 54157-109 Upc 801803 00211 Megafresh Gel Fluoride Tooth

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 54157-109?
  4. Upc 801803 00211 Megafresh Gel Fluoride Tooth Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
54157-109
Proprietary Name:
Upc 801803 00211 Megafresh Gel Fluoride Tooth
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
American Amenities, Inc.
Labeler Code:
54157
Product Label ID:
42824602-9b12-449d-9888-ade5a97ce129
Start Marketing Date: [9]
06-03-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 54157-109?

The NDC code 54157-109 is assigned by the FDA to the product Upc 801803 00211 Megafresh Gel Fluoride Tooth which is product labeled by American Amenities, Inc.. The product's dosage form is . The product is distributed in 9 packages with assigned NDC codes 54157-109-01 17 g in 1 tube , 54157-109-02 24 g in 1 tube , 54157-109-03 43 g in 1 tube , 54157-109-04 78 g in 1 tube , 54157-109-05 85 g in 1 tube , 54157-109-06 130 g in 1 tube , 54157-109-07 181 g in 1 tube , 54157-109-08 200 g in 1 tube , 54157-109-09 4.25 g in 1 pouch . 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 Upc 801803 00211 Megafresh Gel Fluoride Tooth?

Uses: Aids in the prevention of dental cavities

Which are Upc 801803 00211 Megafresh Gel Fluoride Tooth UNII Codes?

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

Which are Upc 801803 00211 Megafresh Gel Fluoride Tooth 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:

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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".