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  4. NDC Product Code: 67659-083 Up And Up Anticavity Toothpaste Multi Function

NDC 67659-083 Up And Up Anticavity Toothpaste Multi Function

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 67659-083?
  5. Up And Up Anticavity Toothpaste Multi Function 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:
67659-083
Proprietary Name:
Up And Up Anticavity Toothpaste Multi Function
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Team Technologies, Inc
Labeler Code:
67659
Product Label ID:
eef7c016-0b43-41cc-8dc5-2e95393f2544
Start Marketing Date: [9]
08-25-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
Flavor(s):
MINT (C73404 - CLEAN MINT FLAVOR)

Code Structure Chart

Product Details

What is NDC 67659-083?

The NDC code 67659-083 is assigned by the FDA to the product Up And Up Anticavity Toothpaste Multi Function which is product labeled by Team Technologies, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 67659-083-02 1 tube in 1 carton / 170 g in 1 tube (67659-083-01). 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 Anticavity Toothpaste Multi Function?

Adults and children 12 years and older     Brush teeth thoroughly, PREFERABLY AFTER EACH MEAL,or at least twice a day,                                                                       or as directed by your dentist. DO NOT SWALLOW Children under 12                                         ASK A dentist or PHYSICIAN Other information                                         PRODUCTS CONTAINING STANNOUS FLUORIDE MAY PRODUCE SURFACE                                                                               STAINING OF THE TEETH. ADEQUATE TOOTHBRUSHING MAY PREVENT                                                                                   THESE STAIN WHICH ARE NOT HARMFUL OR PERMANENT.

Which are Up And Up Anticavity Toothpaste Multi Function UNII Codes?

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

Which are Up And Up Anticavity Toothpaste Multi Function 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 Anticavity Toothpaste Multi Function?

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: 416784 - stannous fluoride 0.454 % (fluoride ion 0.16 % ) Toothpaste
  • RxCUI: 416784 - stannous fluoride 0.00454 MG/MG Toothpaste
  • RxCUI: 416784 - stannous fluoride 0.454 % (fluoride ion 0.14 % ) Toothpaste
  • RxCUI: 416784 - stannous fluoride 0.454 % (fluoride ion 0.15 % ) Toothpaste

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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".