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  4. NDC Product Code: 0273-7007 Perfect Choice

NDC 0273-7007 Perfect Choice

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0273-7007?
  5. Perfect Choice Uses
  6. Active Ingredients UNII Codes
  7. 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:
0273-7007
Proprietary Name:
Perfect Choice
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Young Dental Manufacturing Co 1, Llc.
Labeler Code:
0273
Product Label ID:
a85fc72b-304c-42a7-a4d8-b511e561f78f
Start Marketing Date: [9]
12-22-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
MARSHMALLOW (C82400 - HAPPY HIPPO CAKE)

Product Packages

NDC Code 0273-7007-16

Package Description: 497 g in 1 BOTTLE

Product Details

What is NDC 0273-7007?

The NDC code 0273-7007 is assigned by the FDA to the product Perfect Choice which is product labeled by Young Dental Manufacturing Co 1, Llc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0273-7007-16 497 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 Perfect Choice?

Topical application of APF gel is indicated in the prevention of dental caries.

Which are Perfect Choice UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Perfect Choice?

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: 1297381 - hydrofluoric acid 1 % / phosphoric acid 1.12 % / sodium fluoride 1.8 % Oral Gel
  • RxCUI: 1297381 - hydrofluoric acid 0.01 MG/MG / phosphoric acid 0.0112 MG/MG / sodium fluoride 0.018 MG/MG Oral Gel
  • RxCUI: 1297387 - perfectchoice One Minute 1.23 % Oral Gel
  • RxCUI: 1297387 - hydrofluoric acid 0.01 MG/MG / phosphoric acid 0.0112 MG/MG / sodium fluoride 0.018 MG/MG Oral Gel [Perfect Choice One Minute]
  • RxCUI: 1297387 - Perfect Choice One Minute (hydrofluoric acid 1 % / phosphoric acid 1.12 % / sodium fluoride 1.8 % ) Oral Gel

* 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".