1. Home
  2. Labeler Index
  3. Bellanez
  4. NDC Product Code: 72799-010 De Medicotem Illuminating White Cell Ampoule

NDC 72799-010 De Medicotem Illuminating White Cell Ampoule

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72799-010?
  4. De Medicotem Illuminating White Cell Ampoule 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:
72799-010
Proprietary Name:
De Medicotem Illuminating White Cell Ampoule
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bellanez
Labeler Code:
72799
Product Label ID:
4bb52046-c776-4aa5-842c-e9963093a7c8
Start Marketing Date: [9]
12-01-2018
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 72799-010?

The NDC code 72799-010 is assigned by the FDA to the product De Medicotem Illuminating White Cell Ampoule which is product labeled by Bellanez. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72799-010-02 10 container in 1 carton / 5 ml in 1 container (72799-010-01). 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 De Medicotem Illuminating White Cell Ampoule?

Directions:■ Every morning and night, after using a toner, apply it in a bottle(5ml) evenly over the skin three to four times and make it absorb. Recommended for use within two weeks of release.

Which are De Medicotem Illuminating White Cell Ampoule UNII Codes?

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

Which are De Medicotem Illuminating White Cell Ampoule 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:

* Please review the disclaimer below.

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".