NDC 41442-149 Complexion Corrector Spf20

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:
41442-149
Proprietary Name:
Complexion Corrector Spf20
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Omorovicza Kozmetikai Kft.
Labeler Code:
41442
Start Marketing Date: [9]
01-25-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)

Product Packages

NDC Code 41442-149-01

Package Description: 1 BOTTLE, GLASS in 1 BOX / 30 mL in 1 BOTTLE, GLASS

NDC Code 41442-149-02

Package Description: 50 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 41442-149?

The NDC code 41442-149 is assigned by the FDA to the product Complexion Corrector Spf20 which is product labeled by Omorovicza Kozmetikai Kft.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 41442-149-01 1 bottle, glass in 1 box / 30 ml in 1 bottle, glass, 41442-149-02 50 ml in 1 bottle, pump . 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 Complexion Corrector Spf20?

Appy evenly to face and neck.

Which are Complexion Corrector Spf20 UNII Codes?

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

Which are Complexion Corrector Spf20 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".