NDC 44014-086 Icy Hot Medicated Roll, Large

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:
44014-086
Proprietary Name:
Icy Hot Medicated Roll, Large
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nichiban Company Limited
Labeler Code:
44014
Start Marketing Date: [9]
04-01-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 44014-086-02

Package Description: 150 PATCH in 1 BOX

NDC Code 44014-086-07

Package Description: 1 PATCH in 1 POUCH

Product Details

What is NDC 44014-086?

The NDC code 44014-086 is assigned by the FDA to the product Icy Hot Medicated Roll, Large which is product labeled by Nichiban Company Limited. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 44014-086-02 150 patch in 1 box , 44014-086-07 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 Icy Hot Medicated Roll, Large?

Adults and children over 12 years:tear or cut roll to desired sizecarefully remove backing from one end of strip and place on affected arearemove remaining backing and press into placewear Icy Hot Medicated Roll for up to 8 hoursrepeat as necessary, but no more than 3 to 4 times dailychildren 12 years or younger: ask a doctor

Which are Icy Hot Medicated Roll, Large UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Icy Hot Medicated Roll, Large?

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".