NDC 72490-006 Medicated Compression Sock

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:
72490-006
Proprietary Name:
Medicated Compression Sock
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Textile-based Delivery, Inc.
Labeler Code:
72490
Start Marketing Date: [9]
07-16-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72490-006-01

Package Description: 2 CLOTH in 1 POUCH

NDC Code 72490-006-02

Package Description: 2 CLOTH in 1 POUCH

NDC Code 72490-006-03

Package Description: 2 CLOTH in 1 POUCH

Product Details

What is NDC 72490-006?

The NDC code 72490-006 is assigned by the FDA to the product Medicated Compression Sock which is product labeled by Textile-based Delivery, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 72490-006-01 2 cloth in 1 pouch , 72490-006-02 2 cloth in 1 pouch , 72490-006-03 2 cloth in 1 pouch . 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 Medicated Compression Sock?

Clean and dry affected areaRemove product and put on bodyMaximum use of 8 hours per dayDo not wear more than 4 days per week without doctor consentWash separately for best results

Which are Medicated Compression Sock UNII Codes?

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

Which are Medicated Compression Sock 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:

  • BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)

* 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".