Dynamic Defence Concentrate Anti-ageing Day Spf 15
NDC 49678-1005

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 49678-1005?
  4. Dynamic Defence Concentrate Anti-ageing Day Spf 15 Uses
  5. Active Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Dynamic Defence Concentrate Anti-ageing Day Spf 15 is a OTC MONOGRAPH FINAL-approved product labeled by Sarah Chapman Ltd. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 49678-1005 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
49678-1005
Proprietary Name:
Dynamic Defence Concentrate Anti-ageing Day Spf 15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Sarah Chapman Ltd
Labeler Code:
49678
Product Label ID:
0a9b0058-9b77-434c-8ab9-301f78307b0c
FDA Application Number: [6]
part352
Marketing Category: [8]
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.

Marketing Timeline

Start Marketing Date: [9]
05-04-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I

Code Structure Chart

Product Details

What is NDC 49678-1005?

The NDC code 49678-1005 is assigned by the FDA to the product Dynamic Defence Concentrate Anti-ageing Day Spf 15. This pharmaceutical product is labeled by Sarah Chapman Ltd and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 49678-1005-2. 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?

Other information on the back panel:Fragranced with a subtle hint of jasmine, hyacinth and rose essential oilsUses:This advanced formula day cream for skins already used to high-potency skincare. Essential advice to all clients is to support the skin's natural defense with supercharged levels of vitamins A, C, antioxidants, omega-rich oils and broad spectrum SPF 15.Dynamic Defence Concentrate contains all of these, many in potent double-strength. Revolutionary Renovage TM and Matrixyl TM 3000 peptide combine with triple skin-brighteners and precious iris, rose and jasmine. This helps to give an improved feeling of plumpness, appearance of clarity and restored natural moisture balance.Tips for use: Smooth all over face, neck and chest every morning after Age-Repair Concentrate.

Which are the associated UNII Codes?

The UNII codes for the active 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 FDA Application Number? This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
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".