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  4. NDC Product Code: 11673-682 Up And Up Sensitive Maximum Strength Whitening

NDC 11673-682 Up And Up Sensitive Maximum Strength Whitening

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11673-682?
  4. Up And Up Sensitive Maximum Strength Whitening Uses
  5. Active Ingredients UNII Codes
  6. Inactive 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:
11673-682
Proprietary Name:
Up And Up Sensitive Maximum Strength Whitening
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Target Corporation
Labeler Code:
11673
Product Label ID:
307cfe94-a9d7-492e-999f-2659162fec53
Start Marketing Date: [9]
12-24-2015
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 11673-682?

The NDC code 11673-682 is assigned by the FDA to the product Up And Up Sensitive Maximum Strength Whitening which is product labeled by Target Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11673-682-04 1 tube in 1 carton / 113 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 Up And Up Sensitive Maximum Strength Whitening?

Directionsadults and children 12 years of age and olderapply at least a 1-inch strip of product onto a soft bristle toothbrushbrush teeth thoroughly for at least 1 minute twice a day (morning and evening), and not more than 3 times a day, or as recommended by a dentist or doctor. Make sure to brush all sensitive areas of the teeth. Minimize swallowing. Spit out after brushing.children under 12 years of age: consult a dentist or doctor

Which are Up And Up Sensitive Maximum Strength Whitening UNII Codes?

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

Which are Up And Up Sensitive Maximum Strength Whitening 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 Up And Up Sensitive Maximum Strength Whitening?

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: 1038841 - potassium nitrate 5 % / sodium fluoride 0.15 % Toothpaste
  • RxCUI: 1038841 - potassium nitrate 0.05 MG/MG / sodium fluoride 0.0015 MG/MG Toothpaste
  • RxCUI: 1038841 - K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.0015 MG/MG Toothpaste
  • RxCUI: 1038841 - pot nitrate 0.05 MG/MG / sodium fluoride 0.0015 MG/MG gel Toothpaste
  • RxCUI: 1038841 - Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.0015 MG/MG Toothpaste

* 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".