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  4. NDC Product Code: 67138-533 Polar Frost Cold

NDC 67138-533 Polar Frost Cold

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 67138-533?
  5. Polar Frost Cold 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:
67138-533
Proprietary Name:
Polar Frost Cold
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mettler Electronics Corp.
Labeler Code:
67138
Product Label ID:
35fe8a89-e89a-4e1e-bc89-a445e7bc0d44
Start Marketing Date: [9]
11-11-2002
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)

Code Structure Chart

Product Details

What is NDC 67138-533?

The NDC code 67138-533 is assigned by the FDA to the product Polar Frost Cold which is product labeled by Mettler Electronics Corp.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 67138-533-05 5.43 ml in 1 pouch , 67138-533-15 150 ml in 1 tube , 67138-533-50 500 ml in 1 bottle, pump , 67138-533-64 3785 ml in 1 canister , 67138-533-75 75 ml in 1 bottle, with applicator . 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 Polar Frost Cold?

Adults and children 2 years of age and older:Apply a thin layer to the affected area.Make a second application in 5 minutes.Apply to affected area not more than 3 to 4 times daily.Children under 2 years of age: Do not use, consult a doctor.

Which are Polar Frost Cold UNII Codes?

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

Which are Polar Frost Cold 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 Polar Frost Cold?

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".