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  4. NDC Product Code: 62695-2001 Any Mi Natural Magic Bb No.7

NDC 62695-2001 Any Mi Natural Magic Bb No.7

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62695-2001?
  4. Any Mi Natural Magic Bb No.7 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:
62695-2001
Proprietary Name:
Any Mi Natural Magic Bb No.7
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
K.n.life Co., Ltd.
Labeler Code:
62695
Product Label ID:
d030a64f-e9c5-4c4b-8dd4-abed0f48700c
Start Marketing Date: [9]
03-15-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 62695-2001?

The NDC code 62695-2001 is assigned by the FDA to the product Any Mi Natural Magic Bb No.7 which is product labeled by K.n.life Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62695-2001-1 40 ml in 1 tube . 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 Any Mi Natural Magic Bb No.7?

After foundation, apply small amounts to whole face by tapping until it is absorbed to skin completely

Which are Any Mi Natural Magic Bb No.7 UNII Codes?

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

Which are Any Mi Natural Magic Bb No.7 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".