NDC 76354-614 Elf Broad Spectrum Spf 20 Sunscreen Dark Bb Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76354 - J. A. Cosmetics U.s. Inc
- 76354-614 - Elf Broad Spectrum Spf 20 Sunscreen Dark Bb Cream
Product Packages
NDC Code 76354-614-01
Package Description: 28.5 mL in 1 BOTTLE
Product Details
What is NDC 76354-614?
What are the uses for Elf Broad Spectrum Spf 20 Sunscreen Dark Bb Cream?
Which are Elf Broad Spectrum Spf 20 Sunscreen Dark Bb Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Elf Broad Spectrum Spf 20 Sunscreen Dark Bb Cream 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)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MICA (UNII: V8A1AW0880)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- SODIUM CHLORATE (UNII: T95DR77GMR)
- QUATERNIUM-18 (UNII: O7757NO1VL)
- BENTONITE (UNII: A3N5ZCN45C)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ZINC STEARATE (UNII: H92E6QA4FV)
- TALC (UNII: 7SEV7J4R1U)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALOE ANDONGENSIS LEAF (UNII: N1P4NU25EJ)
- JOJOBA OIL (UNII: 724GKU717M)
- CUCUMBER FRUIT OIL (UNII: R81Y52NPCT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
* 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".