1. Home
  2. Labeler Index
  3. Cj Olive Networks Co., Ltd.
  4. NDC Product Code: 71596-050 Bring Green Fresh Mask Lemon

NDC 71596-050 Bring Green Fresh Mask Lemon

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71596-050?
  4. Bring Green Fresh Mask Lemon 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:
71596-050
Proprietary Name:
Bring Green Fresh Mask Lemon
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cj Olive Networks Co., Ltd.
Labeler Code:
71596
Product Label ID:
26f4f8ce-f747-4248-8acb-4971402c874a
Start Marketing Date: [9]
05-01-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71596-050-01

Package Description: 20 g in 1 POUCH

Product Details

What is NDC 71596-050?

The NDC code 71596-050 is assigned by the FDA to the product Bring Green Fresh Mask Lemon which is product labeled by Cj Olive Networks Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71596-050-01 20 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 Bring Green Fresh Mask Lemon?

Directions:1. Tonify your facial skin after cleansing. 2. After opening pouch, attach mask sheet onto face, avoiding eyes and lips.3. After 10 to 20 minutes, take off the sheet and make be absorbed by lightly tapping it onto face.

Which are Bring Green Fresh Mask Lemon UNII Codes?

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

Which are Bring Green Fresh Mask Lemon 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:

* Please review the disclaimer below.

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".