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  4. NDC Product Code: 28109-010 Acneworx

NDC 28109-010 Acneworx

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 28109-010?
  4. Acneworx Uses
  5. Active Ingredients UNII Codes
  6. 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:
28109-010
Proprietary Name:
Acneworx
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dermworx Incorporated
Labeler Code:
28109
Product Label ID:
43c8f760-7c5c-407c-91ce-674bd13b4ecd
Start Marketing Date: [9]
01-14-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 28109-010?

The NDC code 28109-010 is assigned by the FDA to the product Acneworx which is product labeled by Dermworx Incorporated. The product's dosage form is . The product is distributed in a single package with assigned NDC code 28109-010-06 6 carton in 1 carton / 1 tube in 1 carton (28109-010-01) / 30 ml 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 Acneworx?

Cleanse the skin thoroughly before applying medication. Cover the affected area with a thin layer 1-3 times daily.

Which are Acneworx UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Acneworx?

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:

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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".