NDC 69424-570 Leaders Aquatoning First 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:
69424-570
Proprietary Name:
Leaders Aquatoning First Ampoule Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
69424
Start Marketing Date: [9]
12-01-2015
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 69424-570?

The NDC code 69424-570 is assigned by the FDA to the product Leaders Aquatoning First Ampoule Mask which is product labeled by Sansung Life & Science Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69424-570-01 23 ml in 1 carton . 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 Leaders Aquatoning First Ampoule Mask?

Directions: 1. Open bottle and take out mask by using the stick. 2. Place mask directly on face, contouring it to fit to curves around eyes, nose and mouth. 3. Leave on for 10-20 minutes. 4. Remove mask and gently pat face with fingertips until remaining serum is fully absorbed.Suggested use 2-3 times a week Directions: 1. Open bottle and take out mask by using the stick. 2. Place mask directly on face, contouring it to fit to curves around eyes, nose and mouth. 3. Leave on for 10-20 minutes. 4. Remove mask and gently pat face with fingertips until remaining serum is fully absorbed.Suggested use 2-3 times a week

Which are Leaders Aquatoning First Ampoule Mask UNII Codes?

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

Which are Leaders Aquatoning First 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".