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  4. NDC Product Code: 49726-029 Licenex

NDC 49726-029 Licenex

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49726-029?
  4. Licenex 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:
49726-029
Proprietary Name:
Licenex
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hello Life, Inc.
Labeler Code:
49726
Product Label ID:
50b1c7d6-815f-4b1b-b9d5-e91fbfca9b58
Start Marketing Date: [9]
05-01-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 49726-029?

The NDC code 49726-029 is assigned by the FDA to the product Licenex which is product labeled by Hello Life, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 49726-029-04 1 bottle in 1 carton / 118 ml in 1 bottle, 49726-029-12 1 bottle in 1 carton / 354 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 Licenex?

Apply Licenex to damp hair.  Work into lather and massage into hair and scalp for at least ten minutes.  Pay close attention to nape of neck and behind ears.  Cover hair with shower cap for 30-45 minutes.  Rinse thoroughly and use lice/nit removing comb as directed.  Repeat as needed.

Which are Licenex UNII Codes?

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

Which are Licenex 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".