NDC 72001-0021 Banobagi Vita Cocktail Foil Mask Age

Niacinamide, Adenosine, Glycerin

NDC Product Code 72001-0021

NDC Code: 72001-0021

Proprietary Name: Banobagi Vita Cocktail Foil Mask Age What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Niacinamide, Adenosine, Glycerin What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.


Code Structure
  • 72001 - Banobagi Co., Ltd.
    • 72001-0021 - Banobagi Vita Cocktail Foil Mask Age

NDC 72001-0021-1

Package Description: 300 mL in 1 BOX

NDC Product Information

Banobagi Vita Cocktail Foil Mask Age with NDC 72001-0021 is a a human over the counter drug product labeled by Banobagi Co., Ltd.. The generic name of Banobagi Vita Cocktail Foil Mask Age is niacinamide, adenosine, glycerin. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Banobagi Co., Ltd.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.


Banobagi Vita Cocktail Foil Mask Age Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • NIACINAMIDE 2 g/100mL
  • ADENOSINE .04 g/100mL
  • GLYCERIN 2.8 g/100mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Banobagi Co., Ltd.
Labeler Code: 72001
FDA Application Number: part347 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 01-28-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Banobagi Vita Cocktail Foil Mask Age Product Label Images

Banobagi Vita Cocktail Foil Mask Age Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Niacinamide, adenosine

Inactive Ingredient

Water, Methylpropanediol, Glycerin, Niacinamide, Adenosine, Caprylhydroxamic Acid, Retinyl Palmitate, Thiamine HCl, Riboflavin, Carnitine HCl, Pantothenic Acid, Biotin, Folic Acid, Ascorbic Acid, Tocopherol, Copper Gluconate, Avena Sativa (Oat) Kernel Extract, Copper Tripeptide-1, Sea Water, Allantoin, Trehalose, Dipotassium Glycyrrhizate, Panthenol, Glyceryl Acrylate/Acrylic Acid Copolymer, Propylene Glycol, Carbomer, Hydroxyethylcellulose, Hydroxyacetophenone, Chlorphenesin, Tromethamine, Disodium EDTA

Otc - Purpose

Brightening, Anti Wrinkle

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

1. Thoroughly wash and gently wipe out your face with toner.2. Take out and unfold the mask and apply on your face.3. Remove the mask after 10~20 minutes and let the skin absorb the remaining essence by gently patting the skin

Warnings

1. If abnormal symptoms or side effects such as red spots, swelling, or itching are present in the cosmetics or in the direct sunlight after use, consult a specialist2. Do not use in wounded areas3. Precautions for storage and handling- Keep out of reach of children- Keep away from direct sunlight4. Avoid the use of eye area

Dosage & Administration

For external use only

* Please review the disclaimer below.

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72001-0020
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