NDC 13733-018 Missha Signature Extreme Cover Concealer No.23 Spf30 Pa 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:
13733-018
Proprietary Name:
Missha Signature Extreme Cover Concealer No.23 Spf30 Pa Plus Plus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
13733
Start Marketing Date: [9]
03-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 13733-018?

The NDC code 13733-018 is assigned by the FDA to the product Missha Signature Extreme Cover Concealer No.23 Spf30 Pa Plus Plus which is product labeled by Able C&c Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 13733-018-01 10 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 Missha Signature Extreme Cover Concealer No.23 Spf30 Pa Plus Plus?

INDICATION AND USAGE:After using BB cream or foundation, take an appropriate amount on the brush and apply over the face.Pat with finger tips for better adherence.- TIPS :1) To cover small area: Take an appropriate amount on the brush and dot it on the area and pat with finger tips for better adherence.2) To cover large area: Take an appropriate amount on the brush and spread it over the area and pat with finger tips for better adherence.

Which are Missha Signature Extreme Cover Concealer No.23 Spf30 Pa Plus Plus UNII Codes?

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

Which are Missha Signature Extreme Cover Concealer No.23 Spf30 Pa 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".