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  2. Oral-b Laboratories
  3. NDC Product Code: 0041-0340 Oral-b Minute-foam Banana Splitz

NDC 0041-0340 Oral-b Minute-foam Banana Splitz

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

    1. Product Information
    2. Product Packages
    3. Product Characteristics
    4. What is NDC 0041-0340?
    5. Oral-b Minute-foam Banana Splitz Uses
    6. Active Ingredients UNII Codes
    7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
0041-0340
Proprietary Name:
Oral-b Minute-foam Banana Splitz
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Oral-b Laboratories
Labeler Code:
0041
Product Label ID:
1cecf27b-1f87-4ddd-a675-ac4eba2f7d6b
Start Marketing Date: [9]
05-04-2000
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
BANANA (C73364 - BANANA FLAVOR)
VANILLA (C73421 - VANILLA FLAVOR)

Product Packages

NDC Code 0041-0340-06

Package Description: 165 g in 1 BOTTLE

Product Details

What is NDC 0041-0340?

The NDC code 0041-0340 is assigned by the FDA to the product Oral-b Minute-foam Banana Splitz 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 0041-0340-06 165 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 Banana Splitz?

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

Which are Oral-b Minute-foam Banana Splitz 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 Banana Splitz?

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".