1. Home
  2. Labeler Index
  3. Pine Torte Group Co., Ltd.
  4. NDC Product Code: 69515-030 Treeannsea Eskimo Mella Fertile Soothing Toner

NDC 69515-030 Treeannsea Eskimo Mella Fertile Soothing Toner

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69515-030?
  4. Treeannsea Eskimo Mella Fertile Soothing 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:
69515-030
Proprietary Name:
Treeannsea Eskimo Mella Fertile Soothing Toner
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pine Torte Group Co., Ltd.
Labeler Code:
69515
Product Label ID:
bfcf0028-5eca-43bc-9709-00b5d549cea3
Start Marketing Date: [9]
03-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69515-030-01

Package Description: 200 mL in 1 CARTON

Product Details

What is NDC 69515-030?

The NDC code 69515-030 is assigned by the FDA to the product Treeannsea Eskimo Mella Fertile Soothing Toner which is product labeled by Pine Torte Group Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69515-030-01 200 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 Treeannsea Eskimo Mella Fertile Soothing Toner?

How to use: Apply appropriate amount on the face after cleansing.

Which are Treeannsea Eskimo Mella Fertile Soothing Toner UNII Codes?

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

Which are Treeannsea Eskimo Mella Fertile Soothing 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:

* 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".