NDC 31645-214 Mineral Wear Airbrushing Pressed Powder
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What is NDC 31645-214?
What are the uses for Mineral Wear Airbrushing Pressed Powder?
Which are Mineral Wear Airbrushing Pressed Powder UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Mineral Wear Airbrushing Pressed Powder 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:
- MICA (UNII: V8A1AW0880)
- LAUROYL LYSINE (UNII: 113171Q70B)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- ZINC STEARATE (UNII: H92E6QA4FV)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- O-CYMEN-5-OL (UNII: H41B6Q1I9L)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0)
- GINKGO BILOBA LEAF OIL (UNII: Y5967KO1JH)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- TRICAPRYLIN (UNII: 6P92858988)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- PANAX GINSENG LEAF (UNII: F055A23N6X)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
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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".