NDC 69946-030 Bk Cell 5days Of Secret Snow Whitening

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:
69946-030
Proprietary Name:
Bk Cell 5days Of Secret Snow Whitening
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bnk Co., Ltd.
Labeler Code:
69946
Start Marketing Date: [9]
06-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69946-030-01

Package Description: 25 mL in 1 CELLO PACK

Product Details

What is NDC 69946-030?

The NDC code 69946-030 is assigned by the FDA to the product Bk Cell 5days Of Secret Snow Whitening 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 69946-030-01 25 ml 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 Snow Whitening?

Indications & Usage: 1. After washing, prepare for mask treatment by moisturizing your skin with your regular toner. 2. Wear the mask, follow the cutting leave the eyes and mouth a space after removing plastic cover slip of the one side and then remove the opposite surface plastic cover slip. 3. Leave the mask 15 to 20 minutes and take it off, Massage and dab the face gently let the essence absorb into skin cell well.

Which are Bk Cell 5days Of Secret Snow Whitening UNII Codes?

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

Which are Bk Cell 5days Of Secret Snow Whitening 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".