NDC 0904-5694 Major Extra Strength Cold And Hot Pain Relief Therapy

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:
0904-5694
Proprietary Name:
Major Extra Strength Cold And Hot Pain Relief Therapy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Major Pharmaceuticals
Labeler Code:
0904
Start Marketing Date: [9]
06-30-2013
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 0904-5694-01

Package Description: 1 POUCH in 1 PACKAGE / 5 PATCH in 1 POUCH

Product Details

What is NDC 0904-5694?

The NDC code 0904-5694 is assigned by the FDA to the product Major Extra Strength Cold And Hot Pain Relief Therapy which is product labeled by Major Pharmaceuticals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0904-5694-01 1 pouch in 1 package / 5 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 Major Extra Strength Cold And Hot Pain Relief Therapy?

Directionsadults and children 12 years:remove backing from patch by grasping both ends firmly and gently pulling until backing seperates in middlecarefully remove backing from patchapply one patch to affected areawear one patch up to 8 hoursrepeat as necessary, but no more than 4 times daily children 12 years or younger: consult a doctor

Which are Major Extra Strength Cold And Hot Pain Relief Therapy UNII Codes?

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

Which are Major Extra Strength Cold And Hot Pain Relief Therapy 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 Major Extra Strength Cold And Hot Pain Relief Therapy?

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".