NDC 0041-0345 Oral-b Minute-foam Bubble Gum

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:
0041-0345
Proprietary Name:
Oral-b Minute-foam Bubble Gum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
0041
Start Marketing Date: [9]
05-04-2000
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
BUBBLE GUM (C73368 - BUBBLE GUM FLAVOR)

Code Structure Chart

Product Details

What is NDC 0041-0345?

The NDC code 0041-0345 is assigned by the FDA to the product Oral-b Minute-foam Bubble Gum 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 0041-0345-06 165 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 Bubble Gum?

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

Which are Oral-b Minute-foam Bubble Gum 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 Bubble Gum?

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.

[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".