NDC 64778-1375 Denti-care Topical Fluoride Foam Grape

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
64778-1375
Proprietary Name:
Denti-care Topical Fluoride Foam Grape
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ar Medicom Inc
Labeler Code:
64778
Start Marketing Date: [9]
05-01-2003
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
GRAPE (C73391)

Product Packages

NDC Code 64778-1375-1

Package Description: 125 g in 1 BOTTLE, SPRAY

Product Details

What is NDC 64778-1375?

The NDC code 64778-1375 is assigned by the FDA to the product Denti-care Topical Fluoride Foam Grape which is product labeled by Ar Medicom Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64778-1375-1 125 g in 1 bottle, spray . 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.

Which are Denti-care Topical Fluoride Foam Grape UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Denti-care Topical Fluoride Foam Grape?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1090053 - sodium fluoride 1.76 % / hydrofluoric acid 1.04 % Oral Foam
  • RxCUI: 1090053 - hydrofluoric acid 10.4 MG/ML / sodium fluoride 17.6 MG/ML Oral Foam
  • RxCUI: 1090053 - hydrofluoric acid 1.04 % / sodium fluoride 1.76 % (fluoride ion 1.23 % ) Oral Foam

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[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".