NDC 69346-3001 B Bind Rejuvenating Neoendorphin Mask Pack

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:
69346-3001
Proprietary Name:
B Bind Rejuvenating Neoendorphin Mask Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
69346
Start Marketing Date: [9]
11-01-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 69346-3001?

The NDC code 69346-3001 is assigned by the FDA to the product B Bind Rejuvenating Neoendorphin Mask Pack which is product labeled by Hugel Pharma Co.,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69346-3001-1 30 g in 1 package . 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 B Bind Rejuvenating Neoendorphin Mask Pack?

1.     Soothe your skin with skin lotion after facial cleansing.2.     Draw out the mask from the packet and unfold.3.     Peel off the film4.     Attach the bald side to face and remove the transparent film on the outer part.5.     Enjoy your ordinary life with attached mask after 20~30 minutes.6.     Pat your face for absorbing the essence into the skin.

Which are B Bind Rejuvenating Neoendorphin Mask Pack UNII Codes?

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

Which are B Bind Rejuvenating Neoendorphin Mask Pack 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".