NDC 71673-0008 Dpc Pink Aura Cushion No.23
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71673 - Msco
- 71673-0008 - Dpc Pink Aura Cushion No.23
Product Packages
NDC Code 71673-0008-1
Package Description: 15 g in 1 CONTAINER
Product Details
What is NDC 71673-0008?
What are the uses for Dpc Pink Aura Cushion No.23?
Which are Dpc Pink Aura Cushion No.23 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- AMILOXATE (UNII: 376KTP06K8)
- AMILOXATE (UNII: 376KTP06K8) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- BEMOTRIZINOL (UNII: PWZ1720CBH) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Dpc Pink Aura Cushion No.23 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:
- WATER (UNII: 059QF0KO0R)
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[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".