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  4. NDC Product Code: 51830-019 Lightening Day Cream

NDC 51830-019 Lightening Day Cream

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51830-019?
  4. Lightening Day Cream 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:
51830-019
Proprietary Name:
Lightening Day Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lange Sas
Labeler Code:
51830
Product Label ID:
e62497be-d0ac-4f3e-988f-5d3c2629a08a
Start Marketing Date: [9]
07-18-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 51830-019?

The NDC code 51830-019 is assigned by the FDA to the product Lightening Day Cream which is product labeled by Lange Sas. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51830-019-04 50 mg in 1 container . 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 Lightening Day Cream?

LIGHTENING DAY CREAM LANGEA light and moisturizing cream, to help:Inhibit skin pigmentation,Nourish and moisturize the skin.

Which are Lightening Day Cream UNII Codes?

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

  • POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
  • POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (Active Moiety)

Which are Lightening Day Cream 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".