NDC 69154-020 The Yeon Cmk Pore Blemish Bc 02 Natural Beige

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
69154-020
Proprietary Name:
The Yeon Cmk Pore Blemish Bc 02 Natural Beige
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
69154
Start Marketing Date: [9]
08-01-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 69154-020?

The NDC code 69154-020 is assigned by the FDA to the product The Yeon Cmk Pore Blemish Bc 02 Natural Beige which is product labeled by The Yeon Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69154-020-01 12 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 The Yeon Cmk Pore Blemish Bc 02 Natural Beige?

Indications and usage:1. Push up the formula by around 3mm from the stick, and then apply the formula to the skin as if you draw a line with the stick. Thoroughly put the formula on the skin evenly by using the brush attached to the back of the cosmetic container.2. Especially, if applied to areas, which need cover-up one more time, coverup effects will increase.

Which are The Yeon Cmk Pore Blemish Bc 02 Natural Beige UNII Codes?

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

Which are The Yeon Cmk Pore Blemish Bc 02 Natural Beige 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".