NDC 69017-101 Anti-blemish Matte Primer

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:
69017-101
Proprietary Name:
Anti-blemish Matte Primer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jouer Cosmetics Llc
Labeler Code:
69017
Start Marketing Date: [9]
01-01-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69017-101-02

Package Description: 1 TUBE in 1 BOX / 30 mL in 1 TUBE (69017-101-01)

NDC Code 69017-101-03

Package Description: 1 mL in 1 PACKET

Product Details

What is NDC 69017-101?

The NDC code 69017-101 is assigned by the FDA to the product Anti-blemish Matte Primer which is product labeled by Jouer Cosmetics Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69017-101-02 1 tube in 1 box / 30 ml in 1 tube (69017-101-01), 69017-101-03 1 ml in 1 packet . 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.

Which are Anti-blemish Matte Primer UNII Codes?

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

Which are Anti-blemish Matte Primer 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".