NDC 67659-041 Laura Lynn Anticavity

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
67659-041
Proprietary Name:
Laura Lynn Anticavity
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Team Technologies, Inc
Labeler Code:
67659
Start Marketing Date: [9]
08-29-2006
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
MINT (C73404 - REFRESHING MINT)

Product Packages

NDC Code 67659-041-05

Package Description: 181.4 g in 1 TUBE

Product Details

What is NDC 67659-041?

The NDC code 67659-041 is assigned by the FDA to the product Laura Lynn Anticavity 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 67659-041-05 181.4 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 Laura Lynn Anticavity?

Adults and children        Brush teeth thoroughly, preferably after2 years and older         each meal, or at least twice a day, or as                                         directed by your dentist. Do not swallow.Children under                 To minimize swallowing, use a pea-6 years and older            sized amount and supervise brushing                                         until good habits are established.Children under 2 years   Ask a dentist or physician.

Which are Laura Lynn Anticavity UNII Codes?

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

Which are Laura Lynn Anticavity 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 Laura Lynn Anticavity?

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: 891775 - sodium fluoride 0.243 % Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.00243 MG/MG Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.13 % ) Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.14 % ) Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.15 % ) 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".