NDC 44781-220 Roris Shiny Cc Spf37 Pa Plus Plus Plus

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
44781-220
Proprietary Name:
Roris Shiny Cc Spf37 Pa Plus Plus Plus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Zion Synthetic Fiber Co., Ltd.
Labeler Code:
44781
Start Marketing Date: [9]
02-01-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 44781-220-01

Package Description: 50 g in 1 CARTON

Product Details

What is NDC 44781-220?

The NDC code 44781-220 is assigned by the FDA to the product Roris Shiny Cc Spf37 Pa Plus Plus Plus which is product labeled by Zion Synthetic Fiber Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 44781-220-01 50 g 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 Roris Shiny Cc Spf37 Pa Plus Plus Plus?

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 the direct sunlight.3. Please apply it an adequate quantity evenly on face and throat at the last stage of basic makeup.

Which are Roris Shiny Cc Spf37 Pa Plus Plus Plus UNII Codes?

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

Which are Roris Shiny Cc Spf37 Pa Plus Plus Plus 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".