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  4. NDC Product Code: 44717-535 Natria Acne Treatment

NDC 44717-535 Natria Acne Treatment

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 44717-535?
  4. Natria Acne Treatment 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:
44717-535
Proprietary Name:
Natria Acne Treatment
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wasatch Product Development, Inc.
Labeler Code:
44717
Product Label ID:
2ffec18b-5611-4dc1-95d7-aa0084f93f2e
Start Marketing Date: [9]
06-28-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 44717-535-02

Package Description: 1 TUBE in 1 BOX / 30 mL in 1 TUBE (44717-535-01)

Product Details

What is NDC 44717-535?

The NDC code 44717-535 is assigned by the FDA to the product Natria Acne Treatment which is product labeled by Wasatch Product Development, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 44717-535-02 1 tube in 1 box / 30 ml in 1 tube (44717-535-01). 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 Natria Acne Treatment?

Application: Apply a thin layer evenly over face until completely absorbed. Follow with moisturizer as needed. Use morning and evening.

Which are Natria Acne Treatment UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Natria Acne Treatment?

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".