Freshmint Sensitive
Potassium Nitrate And Sodium Fluoride
New World Imports, Inc
Human Otc Drug
NDC 51824-053Freshmint Sensitive also known as Potassium Nitrate And Sodium Fluoride is a human otc drug labeled by 'New World Imports, Inc'. National Drug Code (NDC) number for Freshmint Sensitive is 51824-053. This drug is available in dosage form of Paste, Dentifrice. The names of the active, medicinal ingredients in Freshmint Sensitive drug includes Potassium Nitrate - 50 mg/g Sodium Fluoride - 2.4 mg/g . The currest status of Freshmint Sensitive drug is Active.
Drug Information:
| Drug NDC: | 51824-053 |
| 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: | Freshmint Sensitive |
| 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: | Potassium Nitrate And Sodium Fluoride |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | New World Imports, Inc |
| 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: | POTASSIUM NITRATE - 50 mg/g
SODIUM FLUORIDE - 2.4 mg/g
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | DENTAL
|
| 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: | OTC MONOGRAPH NOT FINAL |
| 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: | 16 Sep, 2010 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 09 May, 2026 |
| 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. |
| Application Number: | part356 |
| This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null. |
| 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: | New World Imports, Inc
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 1038929
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UPC: | 0085317004729
|
| UPC stands for Universal Product Code. |
| UNII: | RU45X2JN0Z
8ZYQ1474W7
|
| 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 |
|---|
| 51824-053-02 | 1 TUBE in 1 BOX (51824-053-02) / 122 g in 1 TUBE (51824-053-01) | 16 Sep, 2010 | 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 potassium nitrate - antihypersensitivity sodium fluoride - anticavity
Product Elements:
Freshmint sensitive potassium nitrate and sodium fluoride sorbitol silicon dioxide water polyethylene glycol 1500 sodium lauryl sulfate glycerin carboxymethylcellulose sodium titanium dioxide sodium phosphate, tribasic, dodecahydrate saccharin sodium sodium benzoate methylparaben propylparaben d&c yellow no. 10 fd&c blue no. 1 sodium fluoride fluoride ion potassium nitrate nitrate ion mint mint green
Indications and Usage:
Uses builds increasing protection against painful sensitivity of teeth due to cold, heat, acids, sweets or contact. aids in the prevention of dental cavities
Warnings:
Warnings when using this product do not use longer than 4 weeks unless recommended by a dentist or doctor stop and ask a dentist if problem persists or worsens. sensitive teeth may indicate a serious problem that may require prompt care by a dentist
Dosage and Administration:
Directions adults and children 12 years and older: brush teeth for at least one minute, preferably after each meal, or at least twice a day, or as directed by your dentist. be sure to brush sensitive areas. children under 12 years of age: consult a dentist or doctor
Package Label Principal Display Panel:
Toothpaste image.jpg