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  4. NDC Product Code: 52664-006 Elfmineral Blemish Kit Box

NDC 52664-006 Elfmineral Blemish Kit Box

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 52664-006?
  4. Elfmineral Blemish Kit Box 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:
52664-006
Proprietary Name:
Elfmineral Blemish Kit Box
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hangzhou Facecare Cosmetics Co., Ltd.
Labeler Code:
52664
Product Label ID:
57563984-2483-4009-b26d-dcee8d968f0d
Start Marketing Date: [9]
12-01-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 52664-006?

The NDC code 52664-006 is assigned by the FDA to the product Elfmineral Blemish Kit Box which is product labeled by Hangzhou Facecare Cosmetics Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52664-006-01 3.3 g in 1 bottle . 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 Elfmineral Blemish Kit Box?

Uses:Heal and disguise blemishes with the all natural Mineral Blemish Kit.  This translucent powder has active acne fighting ingredients like nature sulfur to treat acne and prevent future breakouts while penetrate deep into the pores to control blackheads.

Which are Elfmineral Blemish Kit Box UNII Codes?

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

Which are Elfmineral Blemish Kit Box 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".