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  4. NDC Product Code: 50410-100 Ra Sence Loe Cure Solu Tion Aloe Mask

NDC 50410-100 Ra Sence Loe Cure Solu Tion Aloe Mask

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50410-100?
  4. Ra Sence Loe Cure Solu Tion Aloe Mask Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50410-100
Proprietary Name:
Ra Sence Loe Cure Solu Tion Aloe Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kimjeongmoon Aloe Co., Ltd.
Labeler Code:
50410
Product Label ID:
d72da453-9f7e-4b1f-b7a8-abef300edaee
Start Marketing Date: [9]
09-01-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 50410-100?

The NDC code 50410-100 is assigned by the FDA to the product Ra Sence Loe Cure Solu Tion Aloe Mask which is product labeled by Kimjeongmoon Aloe Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50410-100-02 10 pouch in 1 carton / 25 ml in 1 pouch (50410-100-01). 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 Ra Sence Loe Cure Solu Tion Aloe Mask?

Directions:1) After cleansing your face, apply skin Toner.2) Remove film and apply it evenly on your face avoiding the eye and mouth area. 3) Remove it after10~20 minutes. Using fingers, gently pat remaining essence into the skin until thoroughly absorbed.

Which are Ra Sence Loe Cure Solu Tion Aloe Mask UNII Codes?

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

Which are Ra Sence Loe Cure Solu Tion Aloe 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".