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  4. NDC Product Code: 69329-600 Dermawerx Zmt Pak

NDC 69329-600 Dermawerx Zmt Pak

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69329-600?
  4. Dermawerx Zmt Pak 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:
69329-600
Proprietary Name:
Dermawerx Zmt Pak
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Patchwerx Labs, Inc.
Labeler Code:
69329
Product Label ID:
24682288-1be4-42af-e054-00144ff88e88
Start Marketing Date: [9]
09-08-2015
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 69329-600?

The NDC code 69329-600 is assigned by the FDA to the product Dermawerx Zmt Pak which is product labeled by Patchwerx Labs, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69329-600-30 1 kit in 1 carton * 113 g in 1 tube (0799-0001-04) * 20 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 Dermawerx Zmt Pak?

Tretinoin gel and cream are indicated for topical application in the treatment of acne vulgaris. The safety and efficacy of the long-term use of this product in the treatment of other disorders have not been established.

Which are Dermawerx Zmt Pak UNII Codes?

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

Which are Dermawerx Zmt Pak 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 Dermawerx Zmt Pak?

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: 106302 - tretinoin 0.025 % Topical Cream
  • RxCUI: 106302 - tretinoin 0.25 MG/ML Topical Cream
  • RxCUI: 1946476 - lanolin 15.7 % / menthol 0.44 % / petrolatum 24 % / zinc oxide 20.6 % Topical Ointment
  • RxCUI: 1946476 - lanolin 0.157 MG/MG / menthol 0.0044 MG/MG / petrolatum 0.24 MG/MG / zinc oxide 0.206 MG/MG Topical Ointment
  • RxCUI: 1946476 - Lanolin 0.157 MG/MG / Menthol 0.0044 MG/MG / Petrolatum 0.24 MG/MG / ZNO 0.206 MG/MG Topical Ointment

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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".