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  4. NDC Product Code: 59078-101 Tonymoly Timeless Ferment Snail Emulsion

NDC 59078-101 Tonymoly Timeless Ferment Snail Emulsion

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59078-101?
  4. Tonymoly Timeless Ferment Snail Emulsion 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:
59078-101
Proprietary Name:
Tonymoly Timeless Ferment Snail Emulsion
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tonymoly Co., Ltd.
Labeler Code:
59078
Product Label ID:
292999b3-5191-00bc-e054-00144ff88e88
Start Marketing Date: [9]
01-14-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 59078-101-01

Package Description: 1 BOTTLE in 1 CARTON / 140 mL in 1 BOTTLE

Product Details

What is NDC 59078-101?

The NDC code 59078-101 is assigned by the FDA to the product Tonymoly Timeless Ferment Snail Emulsion which is product labeled by Tonymoly Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59078-101-01 1 bottle in 1 carton / 140 ml in 1 bottle. 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 Tonymoly Timeless Ferment Snail Emulsion?

Take an adequate amount of the product, gently apply to a face and neck area.

Which are Tonymoly Timeless Ferment Snail Emulsion UNII Codes?

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

Which are Tonymoly Timeless Ferment Snail Emulsion 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".