1. Home
  2. Labeler Index
  3. Fromangel
  4. NDC Product Code: 84176-010 Teenocent Sensitive Tooth

NDC 84176-010 Teenocent Sensitive Tooth

Hydrated Silica,Tricalcium Phosphate,Tocopheryl Acetate Paste, Dentifrice Oral - 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
  7. Active Ingredients UNII Codes
  8. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
84176-010
Proprietary Name:
Teenocent Sensitive Tooth
Non-Proprietary Name: [1]
Hydrated Silica, Tricalcium Phosphate, Tocopheryl Acetate
Substance Name: [2]
Hydrated Silica
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Paste, Dentifrice - A paste formulation intended to clean and/or polish the teeth, and which may contain certain additional agents.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • 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]
    N
    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 a human over the counter drug product labeled by Fromangel. The generic name of Teenocent Sensitive Tooth is hydrated silica, tricalcium phosphate, tocopheryl acetate. The product's dosage form is paste, dentifrice and is administered via oral form. 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

    What are Teenocent Sensitive Tooth Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    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:

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [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 ("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".