1. Home
  2. Labeler Index
  3. C&bcosmetic Co.,ltd.
  4. NDC Product Code: 60611-0006 Abalone Crystaldouble Ex Ampoule

NDC 60611-0006 Abalone Crystaldouble Ex Ampoule

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 60611-0006?
  4. Abalone Crystaldouble Ex 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:
60611-0006
Proprietary Name:
Abalone Crystaldouble Ex Ampoule
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
C&bcosmetic Co.,ltd.
Labeler Code:
60611
Product Label ID:
4a58190e-39d7-38bb-e054-00144ff8d46c
Start Marketing Date: [9]
03-10-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 60611-0006?

The NDC code 60611-0006 is assigned by the FDA to the product Abalone Crystaldouble Ex Ampoule which is product labeled by C&bcosmetic Co.,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60611-0006-1 14 syringe in 1 package / .8 ml in 1 syringe. 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 Abalone Crystaldouble Ex Ampoule?

Take 1EA of ampoule on the palm entirelyMixing well with fingertips and gently tapping along the skin texture for absorptionEven if you do not apply emulsion or cream, you can feel the moistness until next morning*1EA of crystal Double-EX Ampoule is a throwaway product

Which are Abalone Crystaldouble Ex Ampoule UNII Codes?

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

Which are Abalone Crystaldouble Ex 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".