NDC 53208-604 O Hui Perfect Sun Black Ex Broad Spectrum Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53208 - Lg Household And Health Care Inc
- 53208-604 - O Hui Perfect Sun Black Ex Broad Spectrum Spf 50
Product Packages
NDC Code 53208-604-01
Package Description: 1 CONTAINER in 1 CARTON / 50 g in 1 CONTAINER
Product Details
What is NDC 53208-604?
What are the uses for O Hui Perfect Sun Black Ex Broad Spectrum Spf 50?
Which are O Hui Perfect Sun Black Ex Broad Spectrum Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- ENSULIZOLE (UNII: 9YQ9DI1W42) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are O Hui Perfect Sun Black Ex Broad Spectrum Spf 50 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:
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- WATER (UNII: 059QF0KO0R)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- TROMETHAMINE (UNII: 023C2WHX2V)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
- CHRYSIN (UNII: 3CN01F5ZJ5)
- HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- PANTHENOL (UNII: WV9CM0O67Z)
- GALANTHUS NIVALIS SEED (UNII: SJ1FOL985M)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- DISTEARYLDIMONIUM (UNII: 251IW5I21C)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- DIPHENYLSILOXY PHENYL TRIMETHICONE (UNII: I445L28B12)
- MICA (UNII: V8A1AW0880)
* 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".