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  4. NDC Product Code: 67510-0671 Pure-aid Blue Ice Gel

NDC 67510-0671 Pure-aid Blue Ice Gel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 67510-0671?
  4. Pure-aid Blue Ice Gel 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:
67510-0671
Proprietary Name:
Pure-aid Blue Ice Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kareway Product, Inc.`
Labeler Code:
67510
Product Label ID:
e4446218-ded9-2699-e053-2995a90ac74d
Start Marketing Date: [9]
07-20-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 67510-0671-8

Package Description: 226.8 g in 1 JAR

Product Details

What is NDC 67510-0671?

The NDC code 67510-0671 is assigned by the FDA to the product Pure-aid Blue Ice Gel which is product labeled by Kareway Product, Inc.`. The product's dosage form is . The product is distributed in a single package with assigned NDC code 67510-0671-8 226.8 g in 1 jar . 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 Pure-aid Blue Ice Gel?

Clean affected area before applying productAdults and children 2 years and older: apply to the affected area not more than 3 to 4 times dailyChildren under 2 years of age: ask a doctor before using this product

Which are Pure-aid Blue Ice Gel UNII Codes?

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

  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)

Which are Pure-aid Blue Ice Gel 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 Pure-aid Blue Ice Gel?

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:

* 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".