NDC 69946-010 Bk Cell 5days Of Secret Mystic Cleansing

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:
69946-010
Proprietary Name:
Bk Cell 5days Of Secret Mystic Cleansing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
69946
Start Marketing Date: [9]
06-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 69946-010?

The NDC code 69946-010 is assigned by the FDA to the product Bk Cell 5days Of Secret Mystic Cleansing which is product labeled by Bnk Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69946-010-01 20 g in 1 cello pack . 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 Bk Cell 5days Of Secret Mystic Cleansing?

Indications & Usage: 1. After washing, apply facial toner on the face with gentle massage. 2. Duel Mask consists of 2 parts. Firstly remove transparent plastic from the sheet to cover onto the upper face by eyes and nose level and then remove white-pearled plastic after fixing the sheet. Repeat the same process with lower mask for mouth part. 3. Leave up to 40 minutes till dried and lifted thoroughly. You may do your daily life while waiting. 4. Gently take it off from ear area. You can see sebum and debris on the hardened sheet modeled from your face. 5. Rinse your face with lukewarm water. [Professional's Note] Recommended to use cream around your eye & mouth area for better treatment.

Which are Bk Cell 5days Of Secret Mystic Cleansing UNII Codes?

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

Which are Bk Cell 5days Of Secret Mystic Cleansing 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".