Tid Clean Plant
Sodium Chloride
Doctor Choi`s Korea Co., Ltd.
Human Otc Drug
NDC 73666-0580Tid Clean Plant also known as Sodium Chloride is a human otc drug labeled by 'Doctor Choi`s Korea Co., Ltd.'. National Drug Code (NDC) number for Tid Clean Plant is 73666-0580. This drug is available in dosage form of Paste, Dentifrice. The names of the active, medicinal ingredients in Tid Clean Plant drug includes Sodium Chloride - .7 g/100mL . The currest status of Tid Clean Plant drug is Active.
Drug Information:
| Drug NDC: | 73666-0580 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Tid Clean Plant |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Sodium Chloride |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Doctor Choi`s Korea Co., Ltd. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Paste, Dentifrice |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | SODIUM CHLORIDE - .7 g/100mL
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. |
| Marketing Start Date: | 01 Sep, 2022 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 16 Jan, 2025 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | Doctor Choi`s Korea Co., LTD.
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UPC: | 8809296110019
|
| UPC stands for Universal Product Code. |
| UNII: | 451W47IQ8X
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 73666-0580-2 | 1 TUBE in 1 CARTON (73666-0580-2) / 100 mL in 1 TUBE (73666-0580-1) | 01 Sep, 2022 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Purpose prevention of gingivitis
Product Elements:
Tid clean plant sodium chloride sodium chloride chloride ion water glycerin potassium cocoyl glycinate
Indications and Usage:
Uses ? it keeps them white and makes them strong. ? keep your mouth clean. ? refreshes the mouth. ? prevents tooth decay and removes bad breath. ? enhance the aesthetic effect. ? prevention of gingivitis, periodontitis (pyorrhea), prevention of periodontal ? disease, prevention of gum disease
Warnings:
Warnings ? be careful not to swallow, and rinse your mouth thoroughly after use. ? if an abnormality occurs such as damage to the gums or mouth due to the use of this toothpaste, stop using it and consult a doctor or dentist ?when used by children under the age of 6, use a small amount of toothpaste about the size of a pea per serving, and use under the guidance of a guardian to avoid sucking or swallowing. ?if a child under the age of 6 swallows a large amount, consult a doctor or dentist immediately. ?keep out of reach of children under the age of 6
Dosage and Administration:
Directions ?hold an appropriate amount (10~15ml) in your mouth, gargle for about 30 seconds, spit it out, and brush your teeth to clean your teeth.
Package Label Principal Display Panel:
Package label.principal display panel image of carton
Further Questions:
Questions ? 02-363-1502 ? www.doctorchois.com