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  4. NDC Product Code: 67510-0085 Cold And Hot Pain Relief Sleeve

NDC 67510-0085 Cold And Hot Pain Relief Sleeve

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 67510-0085?
  4. Cold And Hot Pain Relief Sleeve 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:
67510-0085
Proprietary Name:
Cold And Hot Pain Relief Sleeve
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kareway Product, Inc.
Labeler Code:
67510
Product Label ID:
1a11d455-c8e5-4ee7-8e0b-6c3eefc29c86
Start Marketing Date: [9]
04-19-2012
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 67510-0085?

The NDC code 67510-0085 is assigned by the FDA to the product Cold And Hot Pain Relief Sleeve 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 67510-0085-4 1 pouch in 1 box / 1 patch in 1 pouch. 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 Cold And Hot Pain Relief Sleeve?

Adults and children over 12 yearsClean and dry affected area.Cut open pouch and remove Sleeve.Remove the clear plastic insert.Pull Sleeve onto knee, large ankle or elbow.Medication is on the colored section of the Sleeve, so the colored section should be placed on the affected area.Pull Sleeve over itself to make medicine touch directly on your skin.Apply one Sleeve to affected area.Repeat as necessary , but no more than 4 times a day.Sleeve should fit snug, but not tight.Children 12 years or younger: ask a doctor

Which are Cold And Hot Pain Relief Sleeve UNII Codes?

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

Which are Cold And Hot Pain Relief Sleeve 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 Cold And Hot Pain Relief Sleeve?

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".