NDC 71619-003 Cellstory Plus Cellplant Meso-care Program (1 Week)

Niacinamide, Adenosine

NDC Product Code 71619-003

NDC CODE: 71619-003

Proprietary Name: Cellstory Plus Cellplant Meso-care Program (1 Week) 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 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.

NDC Code Structure

  • 71619 - Beauren Korea Inc.
    • 71619-003 - Cellstory Plus Cellplant Meso-care Program (1 Week)

NDC 71619-003-01

Package Description: 1 KIT in 1 BOX * 4 CONTAINER in 1 CARTON (71619-160-02) > 1 g in 1 CONTAINER (71619-160-01) * 2 mL in 1 CONTAINER (71619-120-01) * 4 CONTAINER in 1 CARTON (71619-140-02) > 4 g in 1 CONTAINER (71619-140-01) * 1.5 g in 1 CONTAINER (71619-130-01) * 30 g in 1 POUCH (71619-170-01) * 1 mL in 1 CONTAINER (71619-110-01) * 4 CONTAINER in 1 CARTON (71619-100-02) > 1 mL in 1 CONTAINER (71619-100-01) * 4 CONTAINER in 1 CARTON (71619-090-02) > 1 mL in 1 CONTAINER (71619-090-01)

NDC Product Information

Cellstory Plus Cellplant Meso-care Program (1 Week) with NDC 71619-003 is a a human over the counter drug product labeled by Beauren Korea Inc.. The generic name of Cellstory Plus Cellplant Meso-care Program (1 Week) is niacinamide, adenosine. The product's dosage form is kit and is administered via topical form.

Labeler Name: Beauren Korea Inc.

Dosage Form: Kit - A packaged collection of related material.

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.

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)
  • DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • GLYCERETH-26 (UNII: NNE56F2N14)
  • WATER (UNII: 059QF0KO0R)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • WATER (UNII: 059QF0KO0R)
  • WATER (UNII: 059QF0KO0R)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • 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.
  • 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: Beauren Korea Inc.
Labeler Code: 71619
Marketing Category: UNAPPROVED DRUG OTHER - 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: 02-20-2020 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: 12-31-2021 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.

Cellstory Plus Cellplant Meso-care Program (1 Week) Product Label Images

Cellstory Plus Cellplant Meso-care Program (1 Week) 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, glycerin

Inactive Ingredient

See attached product label

Otc - Purpose

See attached product label

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Indications are attached in product label

Warnings

Use it for your own use only.For external use only.Discontinue use if adverse reaction occurs.Contact a physician if symptoms persist.Store at room temperature.Do not reuse it as a disposable product.Please use it immediately after opening.

Dosage & Administration

For topical use only

* Please review the disclaimer below.