NDC 76354-625 Elf Oil Free Flawless Finish Spf 15 Sunscreen Foundation Porcelain
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76354 - J. A. Cosmetics U.s. Inc
- 76354-625 - Elf Oil Free Flawless Finish Spf 15 Sunscreen Foundation Porcelain
Product Packages
NDC Code 76354-625-01
Package Description: 20 mL in 1 BOTTLE
Product Details
What is NDC 76354-625?
What are the uses for Elf Oil Free Flawless Finish Spf 15 Sunscreen Foundation Porcelain?
Which are Elf Oil Free Flawless Finish Spf 15 Sunscreen Foundation Porcelain UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Elf Oil Free Flawless Finish Spf 15 Sunscreen Foundation Porcelain 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)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- BENTONITE (UNII: A3N5ZCN45C)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- MINERAL OIL (UNII: T5L8T28FGP)
- TALC (UNII: 7SEV7J4R1U)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
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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".