NDC 53208-518 Ohui Sunscience Luminous Whitening Sunblock
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53208 - Lg Household And Healthcare, Inc.
- 53208-518 - Ohui Sunscience Luminous Whitening Sunblock
Product Packages
NDC Code 53208-518-02
Package Description: 1 CONTAINER in 1 BOX / 50 mL in 1 CONTAINER (53208-518-01)
Product Details
What is NDC 53208-518?
Which are Ohui Sunscience Luminous Whitening Sunblock UNII Codes?
The UNII codes for the active ingredients in this product are:
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- ENSULIZOLE (UNII: 9YQ9DI1W42) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- BEMOTRIZINOL (UNII: PWZ1720CBH) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ATRACTYLODES JAPONICA ROOT OIL (UNII: EC228KGY00)
- ATRACTYLODES JAPONICA ROOT OIL (UNII: EC228KGY00) (Active Moiety)
Which are Ohui Sunscience Luminous Whitening Sunblock 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)
- ALCOHOL (UNII: 3K9958V90M)
- TROLAMINE (UNII: 9O3K93S3TK)
- TROMETHAMINE (UNII: 023C2WHX2V)
- PANTHENOL (UNII: WV9CM0O67Z)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- PONCIRUS TRIFOLIATA FRUIT (UNII: 44445L49J2)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- HECTORITE (UNII: 08X4KI73EZ)
- ZINC STEARATE (UNII: H92E6QA4FV)
- PHENETHYL BENZOATE (UNII: 0C143929GK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ISODODECANE (UNII: A8289P68Y2)
* 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".