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  4. NDC Product Code: 33261-788 Procomycin

NDC 33261-788 Procomycin

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 33261-788?
  4. Procomycin Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
33261-788
Proprietary Name:
Procomycin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aidarex Pharmaceuticals Llc
Labeler Code:
33261
Product Label ID:
0a94abac-5e83-46bb-94e9-976375b49aa8
Start Marketing Date: [9]
10-01-2010
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 33261-788?

The NDC code 33261-788 is assigned by the FDA to the product Procomycin which is product labeled by Aidarex Pharmaceuticals Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 33261-788-01 15 g in 1 tube . 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 Procomycin?

Clean the affected areaapply a small amount of this product (an amount equal to the surface area of the tip of the finger) on the area 3 times daily.may be covered with a sterile bandagestore at controlled room temperature 15°-30° (59°-86°).

Which are Procomycin UNII Codes?

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

Which are Procomycin 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:

What is the NDC to RxNorm Crosswalk for Procomycin?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1089101 - bacitracin 500 UNT/GM / lidocaine HCl 4 % / neomycin 3.5 MG/GM / polymyxin B 10,000 UNT/GM Topical Cream
  • RxCUI: 1089101 - bacitracin 0.5 UNT/ML / lidocaine hydrochloride 40 MG/ML / neomycin 0.0035 MG/ML / polymyxin B 10 UNT/ML Topical Cream
  • RxCUI: 1089101 - bacitracin 500 UNT / lidocaine HCl 40 MG / neomycin 3.5 MG / polymyxin B 10,000 UNT per GM Topical Cream
  • RxCUI: 1089103 - ProCoMycin 500 UNT/GM / 4 % / 3.5 MG/GM / 10,000 UNT/GM Topical Cream
  • RxCUI: 1089103 - bacitracin 0.5 UNT/ML / lidocaine hydrochloride 40 MG/ML / neomycin 0.0035 MG/ML / polymyxin B 10 UNT/ML Topical Cream [ProCoMycin]

* 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".