NDC 51117-001 Skincare Ldel Retinol Day Broad Spectrum Spf 20
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 51117-001?
What are the uses for Skincare Ldel Retinol Day Broad Spectrum Spf 20?
Which are Skincare Ldel Retinol Day Broad Spectrum Spf 20 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Skincare Ldel Retinol Day Broad Spectrum Spf 20 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- ARGAN OIL (UNII: 4V59G5UW9X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- LEVOMENOL (UNII: 24WE03BX2T)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PETROLATUM (UNII: 4T6H12BN9U)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ETHYLPARABEN (UNII: 14255EXE39)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- PEG-8 STEARATE (UNII: 2P9L47VI5E)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- AMINO ACIDS, SILK (UNII: V0L00EX1IA)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- COUMARIN (UNII: A4VZ22K1WT)
- EUGENOL (UNII: 3T8H1794QW)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- GERANIOL (UNII: L837108USY)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
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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".