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NDC 24653-801 Long Last Makeup 01

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 24653-801?
  4. Long Last Makeup 01 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:
24653-801
Proprietary Name:
Long Last Makeup 01
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Janssen Cosmetics Gmbh
Labeler Code:
24653
Product Label ID:
99dbb0b2-28af-4d23-a5e3-352886cf1ea6
Start Marketing Date: [9]
10-10-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 24653-801?

The NDC code 24653-801 is assigned by the FDA to the product Long Last Makeup 01 which is product labeled by Janssen Cosmetics Gmbh. The product's dosage form is . The product is distributed in a single package with assigned NDC code 24653-801-02 1 bottle, pump in 1 carton / 30 ml in 1 bottle, pump (24653-801-01). 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 Long Last Makeup 01?

This product is used as For external use only. Not to be swallowed. Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water

Which are Long Last Makeup 01 UNII Codes?

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

Which are Long Last Makeup 01 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".