NDC 50184-4700 Shelter Tinted
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 50184-4700?
Which are Shelter Tinted UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM (UNII: D1JT611TNE) (Active Moiety)
Which are Shelter Tinted 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)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARETH-21 (UNII: 53J3F32P58)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- METHYL METHACRYLATE (UNII: 196OC77688)
- DOCOSANOL (UNII: 9G1OE216XY)
- STEARETH-2 (UNII: V56DFE46J5)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- SQUALENE (UNII: 7QWM220FJH)
- RICE BRAN (UNII: R60QEP13IC)
- RUBUS FRUTICOSUS LEAF (UNII: YQ2S06L8S9)
- ENGLISH LAVENDER OIL (UNII: ZBP1YXW0H8)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- CARBOMER 934 (UNII: Z135WT9208)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- OCTYLTRIETHOXYSILANE (UNII: LDC331P08E)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
* 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".