NDC 52553-049 Freshenup Fluoride Double Mint

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:
52553-049
Proprietary Name:
Freshenup Fluoride Double Mint
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
U. S. Nonwovens Corp
Labeler Code:
52553
Start Marketing Date: [9]
08-14-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
MINT (C73404)

Product Packages

NDC Code 52553-049-02

Package Description: 1 TUBE in 1 CARTON / 99.2 g in 1 TUBE

Product Details

What is NDC 52553-049?

The NDC code 52553-049 is assigned by the FDA to the product Freshenup Fluoride Double Mint which is product labeled by U. S. Nonwovens Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52553-049-02 1 tube in 1 carton / 99.2 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 Freshenup Fluoride Double Mint?

Adults and children 2 years and olderbrush teeth thoroughly after meals or at least twice a day or use as directed by a dentist or physicianchildren under 6 yearsto minimize swallowing use a pea sized amount and supervise brushing until good habits are establishedchildren under 2 yearsask a dentist or physician

Which are Freshenup Fluoride Double Mint UNII Codes?

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

Which are Freshenup Fluoride Double Mint 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 Freshenup Fluoride Double Mint?

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: 545626 - sodium monofluorophosphate 0.76 % Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.0076 MG/MG Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )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".