NDC 53208-515 Ohui The First Cell Revolution Age Control Sun Block
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53208 - Lg Household And Healthcare, Inc.
- 53208-515 - Ohui The First Cell Revolution Age Control Sun Block
Product Packages
NDC Code 53208-515-02
Package Description: 1 CONTAINER in 1 BOX / 40 g in 1 CONTAINER (53208-515-01)
Product Details
What is NDC 53208-515?
Which are Ohui The First Cell Revolution Age Control Sun Block UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- ENSULIZOLE (UNII: 9YQ9DI1W42) (Active Moiety)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20) (Active Moiety)
- HYDROXYPROLINE (UNII: RMB44WO89X)
- HYDROXYPROLINE (UNII: RMB44WO89X) (Active Moiety)
Which are Ohui The First Cell Revolution Age Control Sun Block 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- ALCOHOL (UNII: 3K9958V90M)
- ISODODECANE (UNII: A8289P68Y2)
- PANTHENOL (UNII: WV9CM0O67Z)
- METHYL METHACRYLATE (UNII: 196OC77688)
- INULIN (UNII: JOS53KRJ01)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TROMETHAMINE (UNII: 023C2WHX2V)
- CETYL PHOSPHATE (UNII: VT07D6X67O)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
* 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".