NDC 10348-010 Halo Hd Foundation Broad Spectrum Spf 15 Oil Free
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10348 - Smashbox Beauty Cosmetics, Inc
- 10348-010 - Halo Hd Foundation Broad Spectrum Spf 15 Oil Free
Product Packages
NDC Code 10348-010-01
Package Description: 1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE
Product Details
What is NDC 10348-010?
What are the uses for Halo Hd Foundation Broad Spectrum Spf 15 Oil Free?
Which are Halo Hd Foundation Broad Spectrum Spf 15 Oil Free UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Halo Hd Foundation Broad Spectrum Spf 15 Oil Free 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)
- ISODODECANE (UNII: A8289P68Y2)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TRIOCTYLDODECYL CITRATE (UNII: 35X8CT063R)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PALMITIC ACID (UNII: 2V16EO95H1)
- C12-16 ALCOHOLS (UNII: S4827SZE3L)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
* Please review the disclaimer below.
[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".