NDC 52099-8000 Freezin Cold Toast

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:
52099-8000
Proprietary Name:
Freezin Cold Toast
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Q.a. Laboratories
Labeler Code:
52099
Start Marketing Date: [9]
06-12-2012
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 52099-8000-1

Package Description: 141 g in 1 TUBE

Product Details

What is NDC 52099-8000?

The NDC code 52099-8000 is assigned by the FDA to the product Freezin Cold Toast which is product labeled by Q.a. Laboratories. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52099-8000-1 141 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 Freezin Cold Toast?

Directions ¡ use only as directed¡ adults and children 12 years of ageor older: apply to af fected area not morethan 3 to 4 times daily ¡ children under12 years of age: ask a doctor

Which are Freezin Cold Toast UNII Codes?

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

Which are Freezin Cold Toast 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 Freezin Cold Toast?

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: 1300276 - menthol 11 % / methyl salicylate 31 % Topical Cream
  • RxCUI: 1300276 - menthol 110 MG/ML / methyl salicylate 310 MG/ML Topical Cream

* 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".