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  4. NDC Product Code: 78521-020 Curestem Cell Healer C20

NDC 78521-020 Curestem Cell Healer C20

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 78521-020?
  4. Curestem Cell Healer C20 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:
78521-020
Proprietary Name:
Curestem Cell Healer C20
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dnk Corporation Ltd.
Labeler Code:
78521
Product Label ID:
a752bb04-8589-8b87-e053-2a95a90a6252
Start Marketing Date: [9]
06-05-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 78521-020?

The NDC code 78521-020 is assigned by the FDA to the product Curestem Cell Healer C20 which is product labeled by Dnk Corporation Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 78521-020-10 10 vial in 1 box / 2 ml in 1 vial (78521-020-01). 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 Curestem Cell Healer C20?

■ Lift the cap to open. ■ Hold the aluminum cap handle and pull it down to open. ■ Remove the aluminum cap by turning it to the side and then, open the rubber cap. ■ Mix 2 ml of normal saline or purified water and use it on the desired area (face or scalp).

Which are Curestem Cell Healer C20 UNII Codes?

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

Which are Curestem Cell Healer C20 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".