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  4. NDC Product Code: 60949-090 By Pharmicell Lab Luxury Cell Performance Toner

NDC 60949-090 By Pharmicell Lab Luxury Cell Performance Toner

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 60949-090?
  4. By Pharmicell Lab Luxury Cell Performance Toner 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:
60949-090
Proprietary Name:
By Pharmicell Lab Luxury Cell Performance Toner
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pharmicell Co., Ltd.
Labeler Code:
60949
Product Label ID:
b818a187-1954-43d7-ad48-8e0fad8c61d1
Start Marketing Date: [9]
10-01-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 60949-090-01

Package Description: 130 mL in 1 CARTON

Product Details

What is NDC 60949-090?

The NDC code 60949-090 is assigned by the FDA to the product By Pharmicell Lab Luxury Cell Performance Toner which is product labeled by Pharmicell Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60949-090-01 130 ml in 1 carton . 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 By Pharmicell Lab Luxury Cell Performance Toner?

Indications and usage : After wash up, take a proper amount of toner, and spread it evenly over the entire face using a cotton pad for absorption.

Which are By Pharmicell Lab Luxury Cell Performance Toner UNII Codes?

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

Which are By Pharmicell Lab Luxury Cell Performance Toner 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".