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  4. NDC Product Code: 73218-003 Flex24 Pain Pen

NDC 73218-003 Flex24 Pain Pen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73218-003?
  4. Flex24 Pain Pen Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
73218-003
Proprietary Name:
Flex24 Pain Pen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Flex24, Inc.
Labeler Code:
73218
Product Label ID:
94f27aa1-903e-4323-9cd5-6cfc59f7a63a
Start Marketing Date: [9]
08-28-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 73218-003?

The NDC code 73218-003 is assigned by the FDA to the product Flex24 Pain Pen 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 73218-003-01 18 ml in 1 bottle, with applicator . 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 Pen?

Adults and children 2 years of age and older:• Remove plastic top from device and put aside till after treatment• Squeeze device if necessary and apply ointment to the affected area• Repeat as necessary but no more than 3 treatments per dayChildren under 2 years of age, consult a physician.

Which are Flex24 Pain Pen UNII Codes?

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

Which are Flex24 Pain Pen 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 Pen?

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".