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  4. NDC Product Code: 68723-401 Dermesse Pad Treatment 2.0

NDC 68723-401 Dermesse Pad Treatment 2.0

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 68723-401?
  4. Dermesse Pad Treatment 2.0 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:
68723-401
Proprietary Name:
Dermesse Pad Treatment 2.0
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Axia Medical Solutions, Llc
Labeler Code:
68723
Product Label ID:
959c44cd-c067-4bd1-b46b-5fccf4802ef7
Start Marketing Date: [9]
01-01-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 68723-401?

The NDC code 68723-401 is assigned by the FDA to the product Dermesse Pad Treatment 2.0 which is product labeled by Axia Medical Solutions, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68723-401-20 60 lotion in 1 package . 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 Dermesse Pad Treatment 2.0?

Cleanse the skin thoroughly before applying medicationCover the entire affected area with a thin layer one to three times daily.Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or directed by a doctor.If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Which are Dermesse Pad Treatment 2.0 UNII Codes?

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

Which are Dermesse Pad Treatment 2.0 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".