NDC 65364-218 Sunspray
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65364 - Kiss My Face, Llc
- 65364-218 - Sunspray
Product Packages
NDC Code 65364-218-01
Package Description: 100 g in 1 BOTTLE, SPRAY
Product Details
What is NDC 65364-218?
What are the uses for Sunspray?
Which are Sunspray UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Sunspray 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)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- DAUCUS CAROTA SUBSP. CAROTA WHOLE (UNII: Q5AR3Y25MQ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EUCALYPTUS GUNNII LEAF OIL (UNII: 45P837MS5Z)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
- PROPANEDIOL (UNII: 5965N8W85T)
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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".