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  4. NDC Product Code: 71596-045 Botanic Heal Boh Air Jet Daily Mask Collagen

NDC 71596-045 Botanic Heal Boh Air Jet Daily Mask Collagen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71596-045?
  4. Botanic Heal Boh Air Jet Daily Mask Collagen 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:
71596-045
Proprietary Name:
Botanic Heal Boh Air Jet Daily Mask Collagen
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:
ae34d446-33a8-4e2a-940d-04cba38a0fb3
Start Marketing Date: [9]
05-01-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 71596-045?

The NDC code 71596-045 is assigned by the FDA to the product Botanic Heal Boh Air Jet Daily Mask Collagen 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 71596-045-01 25 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 Air Jet Daily Mask Collagen?

Directions:1. After washing the face, apply to tighten the skin texture.2. Take out the mask and evenly attach on the entire face except skin around the eyes and mouth.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 Air Jet Daily Mask Collagen UNII Codes?

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

Which are Botanic Heal Boh Air Jet Daily Mask Collagen 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".