NDC 53208-448 Perioe Lucky Fresh - Cavity Care

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
53208-448
Proprietary Name:
Perioe Lucky Fresh - Cavity Care
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lg Household And Healthcare, Inc.
Labeler Code:
53208
Start Marketing Date: [9]
04-26-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 53208-448-02

Package Description: 1 TUBE in 1 CARTON / 130 g in 1 TUBE (53208-448-01)

Product Details

What is NDC 53208-448?

The NDC code 53208-448 is assigned by the FDA to the product Perioe Lucky Fresh - Cavity Care which is product labeled by Lg Household And Healthcare, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53208-448-02 1 tube in 1 carton / 130 g in 1 tube (53208-448-01). 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 Perioe Lucky Fresh - Cavity Care?

This product is used as Aids in the prevention of : Cavity, Plaque, Bad Breath

Which are Perioe Lucky Fresh - Cavity Care UNII Codes?

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

Which are Perioe Lucky Fresh - Cavity Care 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 Perioe Lucky Fresh - Cavity Care?

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: 1046423 - calcium glycerophosphate 0.13 % / vitamin B6 HCl 0.03 % / sodium monofluorophosphate 0.76 % Toothpaste
  • RxCUI: 1046423 - calcium glycerophosphate 1.3 MG/ML / pyridoxine hydrochloride 0.3 MG/ML / sodium monofluorophosphate 7.6 MG/ML Toothpaste
  • RxCUI: 1046423 - Calcium Glycerophosphate 1.3 MG/ML / vitamin B6 Hydrochloride 0.3 MG/ML / Sodium monofluorophosphate 7.6 MG/ML Toothpaste
  • RxCUI: 1046423 - Calcium Glycerophosphate 1.3 MG/ML / vit-B6 Hydrochloride 0.3 MG/ML / Sodium monofluorophosphate 7.6 MG/ML Toothpaste

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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".