NDC 24653-011 Optimal Tinted Complexion
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 24653-011?
Which are Optimal Tinted Complexion UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Optimal Tinted Complexion 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLUCAMETACIN (UNII: N1EXE5EHAN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- NYLON-12 (UNII: 446U8J075B)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- LAUROYL LYSINE (UNII: 113171Q70B)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TOCOPHEROL (UNII: R0ZB2556P8)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- BENZYL BENZOATE (UNII: N863NB338G)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
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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".