1. Labeler Index
  2. Ventura International Ltd
  3. NDC Product Code: 14783-049 Lbel Paris Regression Jour

NDC 14783-049 Lbel Paris Regression Jour

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

    1. Product Information
    2. Product Packages
    3. What is NDC 14783-049?
    4. Lbel Paris Regression Jour 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:
14783-049
Proprietary Name:
Lbel Paris Regression Jour
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ventura International Ltd
Labeler Code:
14783
Product Label ID:
024de8f0-1d3a-4761-8674-5d1a8ac9133c
Start Marketing Date: [9]
08-15-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 14783-049-61

Package Description: 1 JAR in 1 BOX / 50 g in 1 JAR (14783-049-62)

Product Details

What is NDC 14783-049?

The NDC code 14783-049 is assigned by the FDA to the product Lbel Paris Regression Jour which is product labeled by Ventura International Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 14783-049-61 1 jar in 1 box / 50 g in 1 jar (14783-049-62). 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 Lbel Paris Regression Jour?

Apply smoothly every morning before sun exposure and as needed.apply after cleansing and toning on face and neck.children under 6 months of age: ask a doctor.

Which are Lbel Paris Regression Jour UNII Codes?

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

Which are Lbel Paris Regression Jour 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".