NDC 70959-0002 Hello Care Pore And Sebum Ampoule Mask

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:
70959-0002
Proprietary Name:
Hello Care Pore And Sebum Ampoule Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
World Pack Co., Ltd.
Labeler Code:
70959
Start Marketing Date: [9]
08-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70959-0002-1

Package Description: 10 POUCH in 1 PACKAGE / 25 g in 1 POUCH

Product Details

What is NDC 70959-0002?

The NDC code 70959-0002 is assigned by the FDA to the product Hello Care Pore And Sebum Ampoule Mask which is product labeled by World Pack Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70959-0002-1 10 pouch in 1 package / 25 g in 1 pouch. 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 Hello Care Pore And Sebum Ampoule Mask?

After washing your face, drain off the water and adjust lotion on your face skin.Open the product and attach a mask sheet on your around eyes and full face.Relax for 15-20 minutes and remove it.After getting rid of it, help the rest of liquid on your face to absorb as patting lightly.

Which are Hello Care Pore And Sebum Ampoule Mask UNII Codes?

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

Which are Hello Care Pore And Sebum Ampoule Mask 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".