NDC 53208-524 Ohui Sun Science Sun Block Ex Plus Beige
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53208 - Lg Household And Healthcare, Inc.
- 53208-524 - Ohui Sun Science Sun Block Ex Plus Beige
Product Packages
NDC Code 53208-524-02
Package Description: 1 CONTAINER in 1 BOX / 20 g in 1 CONTAINER (53208-524-01)
Product Details
What is NDC 53208-524?
Which are Ohui Sun Science Sun Block Ex Plus Beige UNII Codes?
The UNII codes for the active ingredients in this product are:
- TALC (UNII: 7SEV7J4R1U)
- TALC (UNII: 7SEV7J4R1U) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ARBUTIN (UNII: C5INA23HXF)
- ARBUTIN (UNII: C5INA23HXF) (Active Moiety)
- ATRACTYLODES JAPONICA ROOT OIL (UNII: EC228KGY00)
- ATRACTYLODES JAPONICA ROOT OIL (UNII: EC228KGY00) (Active Moiety)
Which are Ohui Sun Science Sun Block Ex Plus Beige 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:
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- MICA (UNII: V8A1AW0880)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
* 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".