NDC 54641-004 Flex24 Performance Pen

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:
54641-004
Proprietary Name:
Flex24 Performance Pen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Larasan Pharmaceutical Corporation
Labeler Code:
54641
Start Marketing Date: [9]
04-08-2014
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 54641-004-02

Package Description: 10 mL in 1 BOTTLE, WITH APPLICATOR

Product Details

What is NDC 54641-004?

The NDC code 54641-004 is assigned by the FDA to the product Flex24 Performance Pen which is product labeled by Larasan Pharmaceutical Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54641-004-02 10 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 Performance Pen?

Adults and children over the age of 12:Remove plastic top from device and put aside till after treatmentApply ointment to affected areaRepeat if necessary but no more than 3 treatments a day.Children under 12, consult a doctor before use.

Which are Flex24 Performance Pen UNII Codes?

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

Which are Flex24 Performance 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:

* 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".