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  4. NDC Product Code: 73666-0510 Dr.chois Toothpaste Care

NDC 73666-0510 Dr.chois Toothpaste Care

Silica,Tetrasodium Pyrophosphate,Tocopheryl Acetate Paste, Dentifrice Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73666-0510?
  4. Dr.chois Toothpaste Care Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
73666-0510
Proprietary Name:
Dr.chois Toothpaste Care
Non-Proprietary Name: [1]
Silica, Tetrasodium Pyrophosphate, Tocopheryl Acetate
Substance Name: [2]
.alpha.-tocopherol Acetate; Silicon Dioxide; Sodium Pyrophosphate
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]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Labeler Name: [5]
    Doctor Choi`s Korea Co., Ltd.
    Labeler Code:
    73666
    Product Label ID:
    8ae1f54a-5266-4fcc-9701-129ef7dd7faa
    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]
    09-01-2022
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 73666-0510-2

    Package Description: 1 TUBE in 1 CARTON / 120 g in 1 TUBE (73666-0510-1)

    Product Details

    What is NDC 73666-0510?

    The NDC code 73666-0510 is assigned by the FDA to the product Dr.chois Toothpaste Care which is a human over the counter drug product labeled by Doctor Choi`s Korea Co., Ltd.. The generic name of Dr.chois Toothpaste Care is silica, tetrasodium pyrophosphate, tocopheryl acetate. The product's dosage form is paste, dentifrice and is administered via topical form. The product is distributed in a single package with assigned NDC code 73666-0510-2 1 tube in 1 carton / 120 g in 1 tube (73666-0510-1). 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.chois Toothpaste Care?

    ■ Brushing the teeth with a suitable amount

    What are Dr.chois Toothpaste Care 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.
    • .ALPHA.-TOCOPHEROL ACETATE .1 g/100g - A natural tocopherol and one of the most potent antioxidant tocopherols. It exhibits antioxidant activity by virtue of the phenolic hydrogen on the 2H-1-benzopyran-6-ol nucleus. It has four methyl groups on the 6-chromanol nucleus. The natural d form of alpha-tocopherol is more active than its synthetic dl-alpha-tocopherol racemic mixture.
    • SILICON DIOXIDE 14 g/100g - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
    • SODIUM PYROPHOSPHATE .5 g/100g

    Which are Dr.chois Toothpaste Care UNII Codes?

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

    Which are Dr.chois Toothpaste Care 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

    [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".