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  4. NDC Product Code: 60778-040 Lycoris Rubus Whitening Fluid

NDC 60778-040 Lycoris Rubus Whitening Fluid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 60778-040?
  4. Lycoris Rubus Whitening Fluid 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:
60778-040
Proprietary Name:
Lycoris Rubus Whitening Fluid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lycoris Co., Ltd.
Labeler Code:
60778
Product Label ID:
835b4c6b-3c39-4d51-81a9-29796405dafa
Start Marketing Date: [9]
09-01-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 60778-040?

The NDC code 60778-040 is assigned by the FDA to the product Lycoris Rubus Whitening Fluid which is product labeled by Lycoris Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60778-040-01 135 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 Lycoris Rubus Whitening Fluid?

Indications and usage: 1. Tighten the lid after using it. 2. Don't keep it in the place where the temperature is extremely hot or low and exposed to the direct sunlight. 3. Use it in the evening after washing face.

Which are Lycoris Rubus Whitening Fluid UNII Codes?

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

Which are Lycoris Rubus Whitening Fluid 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".