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  4. NDC Product Code: 11727-007 X-pel Pure Anti-lice

NDC 11727-007 X-pel Pure Anti-lice

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11727-007?
  4. X-pel Pure Anti-lice 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:
11727-007
Proprietary Name:
X-pel Pure Anti-lice
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dermedics Laboratories
Labeler Code:
11727
Product Label ID:
01b92e9e-2b1f-41f7-8188-4b15e81aade8
Start Marketing Date: [9]
04-15-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 11727-007-06

Package Description: 170 g in 1 BOTTLE

Product Details

What is NDC 11727-007?

The NDC code 11727-007 is assigned by the FDA to the product X-pel Pure Anti-lice which is product labeled by Dermedics Laboratories. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11727-007-06 170 g 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 X-pel Pure Anti-lice?

IndicationsFor treatment of pediculosis.Eliminates LiceMakes eggs easy to removeStops itching caused by lice bites

Which are X-pel Pure Anti-lice UNII Codes?

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

Which are X-pel Pure Anti-lice 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".