NDC 10967-642 Revlon Colorstay Liquid Makeup For Oily To Combination Skin

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:
10967-642
Proprietary Name:
Revlon Colorstay Liquid Makeup For Oily To Combination Skin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
10967
Start Marketing Date: [9]
10-27-2014
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Characteristics

Code Structure Chart

Product Details

What is NDC 10967-642?

The NDC code 10967-642 is assigned by the FDA to the product Revlon Colorstay Liquid Makeup For Oily To Combination Skin which is product labeled by Revlon Consumer Products Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10967-642-01 30 ml in 1 bottle, glass . 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 Revlon Colorstay Liquid Makeup For Oily To Combination Skin?

Helps prevent sunburnIf used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Which are Revlon Colorstay Liquid Makeup For Oily To Combination Skin UNII Codes?

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

Which are Revlon Colorstay Liquid Makeup For Oily To Combination Skin 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".