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  4. NDC Product Code: 53241-010 Rachel K Mineral Cc Blemish Balm

NDC 53241-010 Rachel K Mineral Cc Blemish Balm

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 53241-010?
  4. Rachel K Mineral Cc Blemish Balm 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:
53241-010
Proprietary Name:
Rachel K Mineral Cc Blemish Balm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rachel K Cosmetics Pte. Ltd.
Labeler Code:
53241
Product Label ID:
5dc42ab2-cde5-41f5-bb56-0ce9a60fbecb
Start Marketing Date: [9]
01-15-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 53241-010?

The NDC code 53241-010 is assigned by the FDA to the product Rachel K Mineral Cc Blemish Balm which is product labeled by Rachel K Cosmetics Pte. Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53241-010-01 40 g in 1 carton . 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 Rachel K Mineral Cc Blemish Balm?

APPLICATION:1. Apply the cream on your face in five dots to the forehead, nose, two cheeks and chin.2. Blend the cream evenly throughout the whole face in a gentle patting motion.3. Leave the cream in for 2-3 minutes until it disappears.4. Cream will dry into a powdery matte finish and skin will appear dewy with a radiant glow.

Which are Rachel K Mineral Cc Blemish Balm UNII Codes?

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

Which are Rachel K Mineral Cc Blemish Balm 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".