Skin Doctors Photo Age Reverse
NDC 49203-740

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 49203-740?
  4. Skin Doctors Photo Age Reverse 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.

Skin Doctors Photo Age Reverse is a UNAPPROVED DRUG OTHER-approved product labeled by Cat Media Pty Ltd. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 49203-740 and 2 associated package configurations. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
49203-740
Proprietary Name:
Skin Doctors Photo Age Reverse
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Cat Media Pty Ltd
Labeler Code:
49203
Product Label ID:
2e5c0437-9a03-4571-b58d-6742353cd4a2
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.

Marketing Timeline

Start Marketing Date: [9]
04-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I

Code Structure Chart

Product Details

What is NDC 49203-740?

The NDC code 49203-740 is assigned by the FDA to the product Skin Doctors Photo Age Reverse. This pharmaceutical product is labeled by Cat Media Pty Ltd and is currently categorized as listed product. In terms of distribution, this product is available in 2 different package configurations. The associated package NDC(s) include: 49203-740-01, 49203-740-02. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Scientifically shown to reverse years of visible premature ageing including wrinkles, sun spots and imperfections.Problem - Everyday exposure to sunlight accounts for up to 80% of the signs of premature skin ageing. Many of these signs of 'photo-ageing' can begin to develop as early as in our 20's.Solution - Photo Age Reverse™ contains the revolutionary ingredient Venuceane™. Rigorous tests under extreme UV exposure showed that it can reverse some of the worst signs of ageing caused by the sun. It was also seen to prevent the appearance of further photo-ageing of skin.Result - With regular use, Photo Age Reverse™ dramatically reduces the visible signs of premature ageing including existing wrinkles, spots and imperfections. It also helps prevent visible skin ageing so you look younger for longer. In fact tests showed it could save up to 5 years of visible skin ageing in just months.

Which are the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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 & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".