NDC 0041-0341 Oral-b Minute-foam Mellow Mint

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:
0041-0341
Proprietary Name:
Oral-b Minute-foam Mellow Mint
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
0041
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]
05-04-2000
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
WINTERGREEN (C73424 - WINTERGREEN FLAVOR)
VANILLA (C73421 - VANILLA FLAVOR)

Code Structure Chart

Product Details

What is NDC 0041-0341?

The NDC code 0041-0341 is assigned by the FDA to the product Oral-b Minute-foam Mellow Mint which is product labeled by Oral-b Laboratories. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0041-0341-06 165 g in 1 bottle . 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 Oral-b Minute-foam Mellow Mint?

INDICATION AND USE:A topically-applied foaming solution to aid in the prevention of dental caries.

Which are Oral-b Minute-foam Mellow Mint UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Oral-b Minute-foam Mellow Mint?

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: 831834 - sodium fluoride 2.2 % / hydrofluoric acid 0.5 % Oral Foam
  • RxCUI: 831834 - hydrofluoric acid 5 MG/ML / sodium fluoride 22 MG/ML 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.

[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".