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  4. NDC Product Code: 72551-250 Therabreath Fresh Breath

NDC 72551-250 Therabreath Fresh Breath

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 72551-250?
  5. Therabreath Fresh Breath Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72551-250
Proprietary Name:
Therabreath Fresh Breath
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dr. Harold Katz, Llc
Labeler Code:
72551
Product Label ID:
7c3a0bcc-a79f-c413-e053-2991aa0a7f51
Start Marketing Date: [9]
10-04-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - CLEAR)
Flavor(s):
MINT (C73404 - MILD MINT)

Product Packages

NDC Code 72551-250-01

Package Description: 1 TUBE in 1 PACKAGE / 113.5 g in 1 TUBE

NDC Code 72551-250-02

Package Description: 21.3 g in 1 TUBE

Product Details

What is NDC 72551-250?

The NDC code 72551-250 is assigned by the FDA to the product Therabreath Fresh Breath which is product labeled by Dr. Harold Katz, Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 72551-250-01 1 tube in 1 package / 113.5 g in 1 tube, 72551-250-02 21.3 g in 1 tube . 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 Therabreath Fresh Breath?

Adults & Children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision. Children under 2 years of age: Consult a dentist or doctor.

Which are Therabreath Fresh Breath UNII Codes?

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

Which are Therabreath Fresh Breath Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Therabreath Fresh Breath?

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:

* 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.
[Learn More]


* 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".