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  4. NDC Product Code: 75981-213 Anticavity Fluoride Rinse

NDC 75981-213 Anticavity Fluoride Rinse

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75981-213?
  4. Anticavity Fluoride Rinse Uses
  5. Active Ingredients UNII Codes
  6. Inactive 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:
75981-213
Proprietary Name:
Anticavity Fluoride Rinse
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Geiss, Destin + Dunn, Inc
Labeler Code:
75981
Product Label ID:
10cbc8d2-5a7e-42ae-8404-00afd565b709
Start Marketing Date: [9]
08-17-2007
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 75981-213?

The NDC code 75981-213 is assigned by the FDA to the product Anticavity Fluoride Rinse which is product labeled by Geiss, Destin + Dunn, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75981-213-44 .532 l in 1 bottle, plastic . 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 Anticavity Fluoride Rinse?

Use aids in the prevention of dental cavities

Which are Anticavity Fluoride Rinse UNII Codes?

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

Which are Anticavity Fluoride Rinse 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 Anticavity Fluoride Rinse?

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:

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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".