NDC 70098-0010 Siseundeusi Luminant Mask Pack Step2(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:
70098-0010
Proprietary Name:
Siseundeusi Luminant Mask Pack Step2(whitening)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Gk Cosmetic Co., Ltd.
Labeler Code:
70098
Start Marketing Date: [9]
03-09-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70098-0010-1

Package Description: 2 mL in 1 PACKAGE

Product Details

What is NDC 70098-0010?

The NDC code 70098-0010 is assigned by the FDA to the product Siseundeusi Luminant Mask Pack Step2(whitening) which is product labeled by Gk Cosmetic Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70098-0010-1 2 ml 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 Siseundeusi Luminant Mask Pack Step2(whitening)?

After wash your face, take our STEP01 Luminant Umbrella Facial Mask and put it on your face.Take off the sheet after 15 to 20 minutes when it gets absorbed into your skinTap your skin softly for your skin to absorb anything left on the skin.Put STEP02 Luminant Whitening Aqua Creme(2 ml) evenly on your face. When we consider skin turn over period, using the productconsistently for 4 weeks is the most effective way to use the product.

Which are Siseundeusi Luminant Mask Pack Step2(whitening) UNII Codes?

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

Which are Siseundeusi Luminant Mask Pack Step2(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".