NDC 73218-002 Flex24 Pain

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:
73218-002
Proprietary Name:
Flex24 Pain
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Flex24 Inc
Labeler Code:
73218
Start Marketing Date: [9]
08-28-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73218-002-01

Package Description: 7 PATCH in 1 PACKAGE / 1.56 g in 1 PATCH

Product Details

What is NDC 73218-002?

The NDC code 73218-002 is assigned by the FDA to the product Flex24 Pain which is product labeled by Flex24 Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73218-002-01 7 patch in 1 package / 1.56 g 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 Flex24 Pain?

Adults and children over the age of 12:Remove plastic backing from patch and discardApply one patch to affected areaRepeat if necessary, but no more than 3 per dayPatch should be comfortable but not tightSensitive skin – Remove patch under waterChildren under 12: consult a doctor before use

Which are Flex24 Pain UNII Codes?

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

Which are Flex24 Pain 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 Flex24 Pain?

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: 1364993 - camphor 3 % / menthol 2.52 % Medicated Patch
  • RxCUI: 1364993 - camphor 0.03 MG/MG / menthol 0.0252 MG/MG Medicated Patch
  • RxCUI: 1494222 - FLEX24 PERFORMANCE 3 % / 2.52 % Medicated Patch
  • RxCUI: 1494222 - camphor 0.03 MG/MG / menthol 0.0252 MG/MG Medicated Patch [Flex24 Performance]
  • RxCUI: 1494222 - Flex24 Performance (camphor 3 % / menthol 2.52 % ) 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".