NDC 41442-133 Sunkiss Spf15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 41442 - Omorovicza Kozmetikai Kft
- 41442-133 - Sunkiss
Product Characteristics
Product Packages
NDC Code 41442-133-01
Package Description: 1 BOTTLE, GLASS in 1 BOX / 50 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 41442-133?
What are the uses for Sunkiss Spf15?
Which are Sunkiss Spf15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Sunkiss Spf15 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:
- CAPRYLIC/CAPRIC MONO/DIGLYCERIDES (UNII: U72Q2I8C85)
- GLYCERIN (UNII: PDC6A3C0OX)
- SQUALANE (UNII: GW89575KF9)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- STEARYL ETHYLHEXANOATE (UNII: X8707A2274)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HYDROXYSTEARIC ACID (UNII: 933ANU3H2S)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- MICA (UNII: V8A1AW0880)
- GERANIOL (UNII: L837108USY)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- LINALOOL, DL- (UNII: D81QY6I88E)
- APRICOT KERNEL OIL (UNII: 54JB35T06A)
- ACEROLA (UNII: XDD2WEC9L5)
- APPLE (UNII: B423VGH5S9)
- PECTIN (UNII: 89NA02M4RX)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- LACTIC ACID (UNII: 33X04XA5AT)
- 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".