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  4. NDC Product Code: 69109-004 Simplicity Desensitizing

NDC 69109-004 Simplicity Desensitizing

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69109-004?
  4. Simplicity Desensitizing 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:
69109-004
Proprietary Name:
Simplicity Desensitizing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Simplicity Laser, Llc
Labeler Code:
69109
Product Label ID:
8660021c-69c4-49c3-959d-2182c581aa0f
Start Marketing Date: [9]
07-15-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 69109-004?

The NDC code 69109-004 is assigned by the FDA to the product Simplicity Desensitizing which is product labeled by Simplicity Laser, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69109-004-30 30 ml in 1 bottle . 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 Simplicity Desensitizing?

Adults and children 2 years and older: Apply externally to the affected area up to 3-4 times daily.Children under 2 years of age: Consult a doctor.

Which are Simplicity Desensitizing UNII Codes?

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

Which are Simplicity Desensitizing 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 Simplicity Desensitizing?

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".