NDC 64778-0373 Denti-care Denti-foam Topical Sodium Fluoride Bubble Gum
Sodium Fluoride Aerosol, Foam Dental - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64778 - Amd Medicom Inc.
- 64778-0373 - Denti-care Denti-foam
Product Characteristics
Product Packages
NDC Code 64778-0373-3
Package Description: 12 BOTTLE, SPRAY in 1 CASE / 125 g in 1 BOTTLE, SPRAY (64778-0373-1)
Product Details
What is NDC 64778-0373?
What are the uses for Denti-care Denti-foam Topical Sodium Fluoride Bubble Gum?
What are Denti-care Denti-foam Topical Sodium Fluoride Bubble Gum Active Ingredients?
- SODIUM FLUORIDE .0272 g/g - A source of inorganic fluoride which is used topically to prevent dental caries.
Which are Denti-care Denti-foam Topical Sodium Fluoride Bubble Gum UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Denti-care Denti-foam Topical Sodium Fluoride Bubble Gum?
- RxCUI: 248389 - sodium fluoride 2.72 % Oral Foam
- RxCUI: 248389 - sodium fluoride 27.2 MG/ML Oral Foam
- RxCUI: 248389 - sodium fluoride 2.72 % (fluoride ion 1.23 % ) Oral Foam
- RxCUI: 991013 - Denti-Care Denti-Foam 2.72 % Oral Foam
- RxCUI: 991013 - sodium fluoride 27.2 MG/ML Oral Foam [DentiCare Denti Foam]
* Please review the disclaimer below.
Patient Education
Fluoride
Fluoride is used to prevent tooth decay. It is taken up by teeth and helps to strengthen teeth, resist acid, and block the cavity-forming action of bacteria. Fluoride usually is prescribed for children and adults whose homes have water that is not fluoridated (already has fluoride added). This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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* Please review the disclaimer below.
[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.
[10] What is the End Marketing Date? - 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.
[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".