NDC 24653-310 Melafadin Day Protection
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 24653-310?
What are the uses for Melafadin Day Protection?
Which are Melafadin Day Protection UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Melafadin Day Protection 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)
- PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)
- ETHANOLAMINE OLEATE (UNII: U4RY8MRX7C)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- NYLON-12 (UNII: 446U8J075B)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- TRICONTANYL POVIDONE (4 TRICONTANYL BRANCHES/REPEAT) (UNII: N0SS3Q238D)
- BISOCTRIZOLE (UNII: 8NT850T0YS)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- ETHYLHEXYL TRIAZONE (UNII: XQN8R9SAK4)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- DOCOSANOL (UNII: 9G1OE216XY)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- DEXTROSE (UNII: IY9XDZ35W2)
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- UNDECYLENIC ACID (UNII: K3D86KJ24N)
- DIACETYL BOLDINE (UNII: 37727Z7M0I)
- POLYISOBUTYLENE (200000 MW) (UNII: Z6Y02I0591)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TETRASODIUM IMINODISUCCINATE (UNII: GYS41J2635)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TROMETHAMINE (UNII: 023C2WHX2V)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- GERANIOL (UNII: L837108USY)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
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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".