NDC 71596-048 Botanic Heal Boh 360 Lifting So Lution

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:
71596-048
Proprietary Name:
Botanic Heal Boh 360 Lifting So Lution
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cj Olive Networks Co., Ltd.
Labeler Code:
71596
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 71596-048-01

Package Description: 50 mL in 1 POUCH

Product Details

What is NDC 71596-048?

The NDC code 71596-048 is assigned by the FDA to the product Botanic Heal Boh 360 Lifting So Lution 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 71596-048-01 50 ml 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 Botanic Heal Boh 360 Lifting So Lution?

Directions:1. Apply toner to skin after cleansing.2. Take out the mask and stretch the sheet in four directions to fit onto the facial line. Hang the loop onto the ears and attach the sheet closely to the neck.3. Remove the sheet after 10~20 minutes, and gently pat to enhance the absorption of the remaining residue into the skin.

Which are Botanic Heal Boh 360 Lifting So Lution UNII Codes?

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

Which are Botanic Heal Boh 360 Lifting So Lution 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".