NDC 72490-006 Medicated Compression Sock


NDC Product Code 72490-006

NDC 72490-006-01

Package Description: 2 CLOTH in 1 POUCH

NDC 72490-006-02

Package Description: 2 CLOTH in 1 POUCH

NDC 72490-006-03

Package Description: 2 CLOTH in 1 POUCH

NDC Product Information

Medicated Compression Sock with NDC 72490-006 is a a human over the counter drug product labeled by Textile-based Delivery, Inc.. The generic name of Medicated Compression Sock is capsaicin. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Textile-based Delivery, Inc.

Dosage Form: Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Medicated Compression Sock Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • CAPSAICIN .13 1/1

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.


Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Textile-based Delivery, Inc.
Labeler Code: 72490
FDA Application Number: part348 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 07-16-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Medicated Compression Sock Product Label Images

Medicated Compression Sock Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Synthetic Capsaicin 0.13%


Topical Analgesic


For the temporary relief of minor aches and pains of muscles and joints associated with simple backache,arthritis, strains, bruises and sprains.


For external use only

Do Not Use

  • Allergy Alert: if you are allergic to any ingredients of this product or chili peppers contact a doctor before useOn wounds or damaged skinWith, or at same time as, other external analgesic productsWith a heating pad

When Using This Product

  • You may experience a burning sensation which is normal and related to the way the product works. With regular use, this sensation generally diminishes.
  • Do not use immediately before or after activities such as swimming, showering, or sunbathing.Use only as directed.Avoid contact with eyes and mucous membranes or rashes.Wash hands after putting product on body and before touching your face or eyes.

Stop Use And Ask A Doctor If

  • Condition worsens, symptoms persist more than 7 days or clear up and occur again within a few days.rash, itching or excessive skin irritation develops.If pregnant or breastfeeding consult a healthcare professional before use.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.


  • 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

Other Information

Avoid storing product in direct sunlight. Protect product from excessive moisture

Inactive Ingredients

Acrylate copolymer

* Please review the disclaimer below.