NDC 53208-494 Ohui Sun Science Perfect Sunblock Red Ex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53208 - Lg Household And Healthcare, Inc.
- 53208-494 - Ohui Sun Science Perfect Sunblock Red Ex
Product Packages
NDC Code 53208-494-02
Package Description: 1 CONTAINER in 1 BOX / 60 mL in 1 CONTAINER (53208-494-01)
Product Details
What is NDC 53208-494?
Which are Ohui Sun Science Perfect Sunblock Red Ex UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Ohui Sun Science Perfect Sunblock Red Ex 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:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- WATER (UNII: 059QF0KO0R)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- VANILLA (UNII: Q74T35078H)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- FRUIT (UNII: C2AIY4ERZC)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- HECTORITE (UNII: 08X4KI73EZ)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ZINC STEARATE (UNII: H92E6QA4FV)
- SORBITAN (UNII: 6O92ICV9RU)
- PANTHENOL (UNII: WV9CM0O67Z)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- TROLAMINE (UNII: 9O3K93S3TK)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- TALC (UNII: 7SEV7J4R1U)
- ETHYLPARABEN (UNII: 14255EXE39)
- MICA (UNII: V8A1AW0880)
- CHROMIUM (UNII: 0R0008Q3JB)
* 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".