NDC 64772-300 Primer

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:
64772-300
Proprietary Name:
Primer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Derma Sciences Canada, Inc.
Labeler Code:
64772
Start Marketing Date: [9]
05-10-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 64772-300-03

Package Description: 1 DRESSING in 1 BOX

NDC Code 64772-300-04

Package Description: 1 DRESSING in 1 BOX

NDC Code 64772-300-05

Package Description: 60 DRESSING in 1 BOX

NDC Code 64772-300-06

Package Description: 60 DRESSING in 1 BOX

Product Details

What is NDC 64772-300?

The NDC code 64772-300 is assigned by the FDA to the product Primer which is product labeled by Derma Sciences Canada, Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 64772-300-03 1 dressing in 1 box , 64772-300-04 1 dressing in 1 box , 64772-300-05 60 dressing in 1 box , 64772-300-06 60 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 Primer?

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).Continue bandaging to just below the knees (STEP 2).Apply an elastic adhesive bandage (STEP 3).

Which are Primer UNII Codes?

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

Which are Primer 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".