NDC 52664-003 Elf Tinted Moisturizer Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52664 - Hangzhou Facecare Cosmetics Co., Ltd.
- 52664-003 - Elf Tinted Moisturizer Spf 15
Product Packages
NDC Code 52664-003-01
Package Description: 12 g in 1 BOTTLE
Product Details
What is NDC 52664-003?
What are the uses for Elf Tinted Moisturizer Spf 15?
Which are Elf Tinted Moisturizer Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Elf Tinted Moisturizer Spf 15 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:
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MICA (UNII: V8A1AW0880)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- KAOLIN (UNII: 24H4NWX5CO)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TALC (UNII: 7SEV7J4R1U)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- WHITE WAX (UNII: 7G1J5DA97F)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- DIETHANOLAMINE CETYL PHOSPHATE (UNII: 4UG0316V9S)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TROLAMINE (UNII: 9O3K93S3TK)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ETHYLPARABEN (UNII: 14255EXE39)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- WATER (UNII: 059QF0KO0R)
* 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".