1. Home
  2. Labeler Index
  3. Reliamed
  4. NDC Product Code: 52641-300 Reliamed

NDC 52641-300 Reliamed

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 52641-300?
  4. Reliamed Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
52641-300
Proprietary Name:
Reliamed
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Reliamed
Labeler Code:
52641
Product Label ID:
8807c7be-cafd-4b30-85c4-1146efc1162e
Start Marketing Date: [9]
08-13-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 52641-300?

The NDC code 52641-300 is assigned by the FDA to the product Reliamed which is product labeled by Reliamed. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 52641-300-03 1 dressing in 1 box , 52641-300-04 1 dressing in 1 box . 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 Reliamed?

Begin bandaging at base of toes, without pressure, keeping foot and leg at right angle. Continue bandaging beyond ankle, doubling back to ensure molding to contours of leg (STEP 1).Complete bandaging to just below the knee (STEP 2).Apply an elastic adhesive bandage (STEP 3).

Which are Reliamed UNII Codes?

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

Which are Reliamed 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".