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  4. NDC Product Code: 84176-010 Teenocent Sensitive Tooth

NDC 84176-010 Teenocent Sensitive Tooth

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 84176-010?
  5. Teenocent Sensitive Tooth Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Get all the details for National Drug Code (NDC) 84176-010 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
84176-010
Proprietary Name:
Teenocent Sensitive Tooth
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Fromangel
Labeler Code:
84176
Product Label ID:
1a802dba-be85-b83e-e063-6294a90a96a3
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date: [9]
05-01-2024
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Code Structure Chart

Product Details

What is NDC 84176-010?

The NDC code 84176-010 is assigned by the FDA to the product Teenocent Sensitive Tooth which is product labeled by Fromangel. The product's dosage form is . The product is distributed in a single package with assigned NDC code 84176-010-02 1 tube in 1 carton / 80 g in 1 tube (84176-010-01). 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 Teenocent Sensitive Tooth?

Use(s)■ Keep your teeth white and strong■ Keep your mouth clean■ Refresh the inside of the mouth■ Prevents tooth decay and Removes bad breath■ Increases aesthetic effect■ Prevention of gingivitis and periodontal inflammation (alveolar abscess)■ Prevention of periodontal disease■ Prevention of gum disease and Removal of plaque (anti-prag)■ Protection of sensitive teeth

Which are Teenocent Sensitive Tooth UNII Codes?

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

Which are Teenocent Sensitive Tooth 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.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".