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  4. NDC Product Code: 75908-017 Periogel

NDC 75908-017 Periogel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 75908-017?
  5. Periogel 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:
75908-017
Proprietary Name:
Periogel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Qnt Anderson, Llc
Labeler Code:
75908
Product Label ID:
30f97d9b-7551-499f-b3bb-5a658bd3a493
Start Marketing Date: [9]
04-01-2011
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
WINTERGREEN (C73424)

Code Structure Chart

Product Details

What is NDC 75908-017?

The NDC code 75908-017 is assigned by the FDA to the product Periogel which is product labeled by Qnt Anderson, Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 75908-017-28 1 tube in 1 carton / 28.3 g in 1 tube, 75908-017-85 1 tube in 1 carton / 85 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 Periogel?

Apply several drops to the affected area of the mouth.Allow medication to remain in place at least 1 minute and then spit out.Use up to 4 times daily after meals and at bedtime or as directed by a dentist or doctor.Children under 12 years of age should be supervised in the use of this product.Children under 2 years of age:Consult a dentist or doctor.

Which are Periogel UNII Codes?

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

Which are Periogel 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 Periogel?

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".