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  4. NDC Product Code: 49678-1005 Dynamic Defence Concentrate Anti-ageing Day Spf 15

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

View Dosage, Usage, Ingredients, Routes, UNII

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.

Get all the details for National Drug Code (NDC) 49678-1005 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

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

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 which is product labeled by Sarah Chapman Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49678-1005-2 1 bottle, pump in 1 carton / 40 ml in 1 bottle, pump (49678-1005-1). 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 Dynamic Defence Concentrate Anti-ageing Day Spf 15?

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 Dynamic Defence Concentrate Anti-ageing Day Spf 15 UNII Codes?

The UNII codes for the active 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.

[6] 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.

[8] 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.

[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, 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".