NDC 76119-1170 Mally Perfect Prep Poreless Primer
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 76119-1170?
What are the uses for Mally Perfect Prep Poreless Primer?
Which are Mally Perfect Prep Poreless Primer UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Mally Perfect Prep Poreless 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- CORN OIL (UNII: 8470G57WFM)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- POLYETHYLENE GLYCOL 900 (UNII: UEP843BRCQ)
- POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- PEG-10 RAPESEED STEROL (UNII: 258O76T85M)
- CERAMIDE 2 (UNII: C04977SRJ5)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C RED NO. 17 (UNII: ND733RX3JN)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PENTAERYTHRITYL TETRAISOSTEARATE (UNII: 9D7IK5483F)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
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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".