Charmzone Natural Skinade Bb Cream (spf20 Pa)
NDC 22201-1001

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 22201-1001?
  4. Charmzone Natural Skinade Bb Cream (spf20 Pa) 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.

Charmzone Natural Skinade Bb Cream (spf20 Pa) is a OTC MONOGRAPH FINAL-approved product labeled by Charmzone Co Ltd. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 22201-1001 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
22201-1001
Proprietary Name:
Charmzone Natural Skinade Bb Cream (spf20 Pa)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Charmzone Co Ltd
Labeler Code:
22201
Product Label ID:
d81ecc9d-2dfc-4778-8219-d0a697be371c
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]
12-01-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I

Code Structure Chart

Product Details

What is NDC 22201-1001?

The NDC code 22201-1001 is assigned by the FDA to the product Charmzone Natural Skinade Bb Cream (spf20 Pa). This pharmaceutical product is labeled by Charmzone Co 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: 22201-1001-1. 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?

This product is used as Benefits of Natural Skinade B.B Cream:1. Foundation Effect: Cover up skin blemishes naturally and make your skin look natural and bright by correcting your skin tone naturally, almost similar to your actual skin tone.2. Make-up Base Effect: Cover up your skin tone clearly and naturally and maintain its fresh makeup for long by improving its makeup fitness to the skin.3. UV Protection (SPF20/PA++): By blocking the UV A and B at the same time, it protects your skin from the sunlight and harmful environments.4. Moisturizing and Nourishment: Its small molecule Sodium Hyaluronic Acid, radicle extract and fermented soybean supply moisture to the skin to maintain its softness and freshness.5. Skin Soothing and Sebum Control: By containing mushroom and persimmon leaf extract, it eliminates extra sebum and alleviates the skin to keep your skin fresh all day long.

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".