NDC 65923-901 Family Care Back Pain 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:
65923-901
Proprietary Name:
Family Care Back Pain Therapy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
United Exchange Corp
Labeler Code:
65923
Start Marketing Date: [9]
12-27-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 65923-901-37

Package Description: 1 PACKET in 1 BOX / 2 PATCH in 1 PACKET

Product Details

What is NDC 65923-901?

The NDC code 65923-901 is assigned by the FDA to the product Family Care Back Pain Therapy which is product labeled by United Exchange Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 65923-901-37 1 packet in 1 box / 2 patch in 1 packet. 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 Family Care Back Pain Therapy?

DirectionsAdults and children 12 years and over apply to affected area; change patch 1 to 2 times dailyChildren under 12 years, consult doctor before useHow to apply:Clean and dry affected areaCut open pouch and remove patchRemove protective film and apply directly to area of painApply to affected area not more than 3 times dailyWash hands with soap after applying patchReseal pouch containing unused patches

Which are Family Care Back Pain Therapy UNII Codes?

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

Which are Family Care Back Pain 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 Family Care Back Pain 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:
  • RxCUI: 853132 - camphor 80 MG / capsicum 16 MG / menthol 24 MG Medicated Patch
  • RxCUI: 853132 - camphor 80 MG / Capsicum extract 16 MG / menthol 24 MG Medicated Patch

* 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".