NDC 80134-050 Brillie Ultimate Soothing Sun Shield
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80134 - Inhanzglobal Co.,ltd
- 80134-050 - Brillie Ultimate Soothing Sun Shield
Product Packages
NDC Code 80134-050-02
Package Description: 1 TUBE in 1 BOX / 50 mL in 1 TUBE (80134-050-01)
Product Details
What is NDC 80134-050?
Which are Brillie Ultimate Soothing Sun Shield UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- SULISOBENZONE (UNII: 1W6L629B4K)
- SULISOBENZONE (UNII: 1W6L629B4K) (Active Moiety)
Which are Brillie Ultimate Soothing Sun Shield 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:
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- HYDROGENATED POLYDECENE TYPE I (UNII: U333RI6EB7)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CYDONIA OBLONGA SEED (UNII: JXU526QH1V)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SHEA BUTTER (UNII: K49155WL9Y)
- JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- TROLAMINE (UNII: 9O3K93S3TK)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- EUROPEAN HAZELNUT OIL (UNII: 8RQ2839AVG)
- GLYCERETH-26 (UNII: NNE56F2N14)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- NYLON-12 (UNII: 446U8J075B)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PEG/PPG-19/19 DIMETHICONE (UNII: EHH90CO7TL)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATERMELON (UNII: 231473QB6R)
- CITRULLINE (UNII: 29VT07BGDA)
* 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".