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  4. NDC Product Code: 52426-520 Myxcin-c

NDC 52426-520 Myxcin-c

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 52426-520?
  4. Myxcin-c 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:
52426-520
Proprietary Name:
Myxcin-c
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Phoenix Global Supply Group, Inc.
Labeler Code:
52426
Product Label ID:
94be7c2a-b372-4f43-8cf1-f382ab629ebe
Start Marketing Date: [9]
02-15-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 52426-520?

The NDC code 52426-520 is assigned by the FDA to the product Myxcin-c which is product labeled by Phoenix Global Supply Group, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52426-520-05 1 bottle in 1 carton / 236.5 ml in 1 bottle. 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 Myxcin-c?

For first aid antiseptic use in adults and children 2 years of age and older:clean the affected areapump a small amount of the product on the affected area 1 to 3 times dailywipe off excess with sterile gauzemay be covered with a sterile bandageif bandaged, let dry firstFor minor wound cleansing in adults and children 2 years of age and older:to clean dirt and debris, pump a small amount of the product on the affected area and wipe off with sterile gauzeChildren under 2 years of age: consult a doctor

Which are Myxcin-c UNII Codes?

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

Which are Myxcin-c 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:

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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".