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  4. NDC Product Code: 82989-030 Dr.noah Toothpaste Tablets

NDC 82989-030 Dr.noah Toothpaste Tablets

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82989-030?
  4. Dr.noah Toothpaste Tablets Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
82989-030
Proprietary Name:
Dr.noah Toothpaste Tablets
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Project Noah Inc.
Labeler Code:
82989
Product Label ID:
3fec6cda-62cc-4e13-a100-1411681c5bbc
Start Marketing Date: [9]
10-01-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 82989-030?

The NDC code 82989-030 is assigned by the FDA to the product Dr.noah Toothpaste Tablets which is product labeled by Project Noah Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 82989-030-01 30 paste, dentifrice in 1 cello pack , 82989-030-02 180 paste, dentifrice in 1 cello pack . 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 Dr.noah Toothpaste Tablets?

■ Adults and children 6 years of age and older: Chew tablet briefly before brushing teeth thoroughly at least twice a day, after each meal or as directed by a dentist or doctor. Instruct children under 12 years of age in good brushing and rinsing habits (to minimize swallowing). Children under 6 years of age: Do not use unless directed by a dentist or doctor.

Which are Dr.noah Toothpaste Tablets UNII Codes?

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

Which are Dr.noah Toothpaste Tablets 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:

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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".