1. Home
  2. Labeler Index
  3. Elevate Oral Care
  4. NDC Product Code: 57511-0120 Just Right 5000

NDC 57511-0120 Just Right 5000

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 57511-0120?
  5. Just Right 5000 Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
57511-0120
Proprietary Name:
Just Right 5000
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Elevate Oral Care
Labeler Code:
57511
Product Label ID:
90b97c2c-07af-2d33-e053-2995a90ad7e6
Start Marketing Date: [9]
01-01-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
Shape:
ROUND (C48348)
Flavor(s):
BUBBLE GUM (C73368 - AND MINT)

Product Packages

NDC Code 57511-0120-8

Package Description: 91 g in 1 TUBE

Product Details

What is NDC 57511-0120?

The NDC code 57511-0120 is assigned by the FDA to the product Just Right 5000 which is product labeled by Elevate Oral Care. The product's dosage form is . The product is distributed in a single package with assigned NDC code 57511-0120-8 91 g in 1 tube . 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 Just Right 5000?

Helps protect against cavities

Which are Just Right 5000 UNII Codes?

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

Which are Just Right 5000 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:

* Please review the disclaimer below.

Patient Education

Fluoride


Fluoride is used to prevent tooth decay. It is taken up by teeth and helps to strengthen teeth, resist acid, and block the cavity-forming action of bacteria. Fluoride usually is prescribed for children and adults whose homes have water that is not fluoridated (already has fluoride added). This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
[Learn More]


* 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".