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  4. NDC Product Code: 65923-012 Family Care Thera Flex

NDC 65923-012 Family Care Thera Flex

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 65923-012?
  4. Family Care Thera Flex Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
65923-012
Proprietary Name:
Family Care Thera Flex
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
United Exchange Corp.
Labeler Code:
65923
Product Label ID:
e9753542-1b08-4dcc-a0f5-299384b44227
Start Marketing Date: [9]
11-15-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 65923-012?

The NDC code 65923-012 is assigned by the FDA to the product Family Care Thera Flex 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 65923-012-01 1 patch in 1 pouch / 1 mg in 1 patch. 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 Thera Flex?

Directions: Adult 18 years and olderclean and dry affected arearemove patch from backing film and apply to skin (see illustration)apply one patch to the affected area and leave in place for up to 8 to 12 hoursif pains last after using the first patch, a second patch may be applied for up to another 8 to 12 hoursonly use on patch at a time do not use more than 2 patches per daydo not use for more than 3 days in a rowChildren under 18 years of age: do not use

Which are Family Care Thera Flex UNII Codes?

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

Which are Family Care Thera Flex 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:

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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".