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  4. NDC Product Code: 76173-1003 Vita Fresh

NDC 76173-1003 Vita Fresh

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 76173-1003?
  5. Vita Fresh Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
76173-1003
Proprietary Name:
Vita Fresh
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cellinbio Co Ltd
Labeler Code:
76173
Product Label ID:
6a708e50-ab4c-4eab-954d-f24780a324a3
Start Marketing Date: [9]
07-27-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - GREEN AND BLACK)

Code Structure Chart

Product Details

What is NDC 76173-1003?

The NDC code 76173-1003 is assigned by the FDA to the product Vita Fresh which is product labeled by Cellinbio Co Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76173-1003-2 1 tube in 1 box / 150 g in 1 tube (76173-1003-1). 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 Vita Fresh?

This product is used as Anticaries

Which are Vita Fresh UNII Codes?

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

Which are Vita Fresh 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 Vita Fresh?

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: 1117211 - sodium monofluorophosphate 0.75 % Toothpaste
  • RxCUI: 1117211 - sodium monofluorophosphate 0.0075 MG/MG Toothpaste
  • RxCUI: 1117211 - sodium monofluorophosphate 0.75 % (fluoride 0.13 % ) Toothpaste

* 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".