NDC 45634-461 No Makeup Lipstick (wine) Spf15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 45634 - N.v Perricone Llc
- 45634-461 - No Makeup Lipstick (wine) Spf15
Product Characteristics
Product Packages
NDC Code 45634-461-52
Package Description: 24.7 g in 1 APPLICATOR
Product Details
What is NDC 45634-461?
Which are No Makeup Lipstick (wine) Spf15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are No Makeup Lipstick (wine) Spf15 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:
- VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
- PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
- PHYTOSTERYL MACADAMIATE (UNII: 233VSF903M)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
- CERESIN (UNII: Q1LS2UJO3A)
- VANILLIN (UNII: CHI530446X)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- TRIDECYL TRIMELLITATE (UNII: FY36J270ES)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- DIMER DILINOLEYL DIMER DILINOLEATE (UNII: 0E2D5DBT7M)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PEG-8 BEESWAX (UNII: 3C1QUF1TIR)
- C10-30 CHOLESTEROL/LANOSTEROL ESTERS (UNII: 137SL7IL0Y)
- ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)
- HYDROGENATED JOJOBA OIL (UNII: 7F674YQ5SO)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- JOJOBA OIL (UNII: 724GKU717M)
- SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ARGANIA SPINOSA SEED (UNII: 8H7X7XB54H)
- .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
- PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- POLYGLYCERYL-2 DIISOSTEARATE (UNII: DG195GP57P)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- D&C RED NO. 6 (UNII: 481744AI4O)
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[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".