1. Home
  2. Labeler Index
  3. Coson Co., Ltd.
  4. NDC Product Code: 62171-080 Gd11 Advanced Lab Energy Ampoule

NDC 62171-080 Gd11 Advanced Lab Energy Ampoule

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62171-080?
  4. Gd11 Advanced Lab Energy 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:
62171-080
Proprietary Name:
Gd11 Advanced Lab Energy Ampoule
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Coson Co., Ltd.
Labeler Code:
62171
Product Label ID:
b213e53f-ee2f-40cd-9b5b-11bfe4058c9f
Start Marketing Date: [9]
07-01-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 62171-080?

The NDC code 62171-080 is assigned by the FDA to the product Gd11 Advanced Lab Energy Ampoule which is product labeled by Coson Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62171-080-02 5 container in 1 carton / 8 ml in 1 container (62171-080-01). 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 Gd11 Advanced Lab Energy Ampoule?

Directions: Hold the bottom of ampoule, twist it to the end Shake the ampoule from left to right and mix the stem cell culture powder derived from Human Cord Blood Stem Cell with ampoule until its color changed to purple. Pump out 3-4 times on the palms and apply all over the face.

Which are Gd11 Advanced Lab Energy Ampoule UNII Codes?

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

Which are Gd11 Advanced Lab Energy 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".