NDC 59351-0332 Rimmel London Moisture Renew Lipgloss - Peach Fusion (117)
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What is NDC 59351-0332?
What are the uses for Rimmel London Moisture Renew Lipgloss - Peach Fusion (117)?
Which are Rimmel London Moisture Renew Lipgloss - Peach Fusion (117) 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)
Which are Rimmel London Moisture Renew Lipgloss - Peach Fusion (117) 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:
- MINERAL OIL (UNII: T5L8T28FGP)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- LANOLIN (UNII: 7EV65EAW6H)
- ETHYLENE (UNII: 91GW059KN7)
- ALUMINUM (UNII: CPD4NFA903)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ISOPROPYLPARABEN (UNII: A6EOX47QK0)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- SORBITAN (UNII: 6O92ICV9RU)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PALMITIC ACID (UNII: 2V16EO95H1)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SULFATE ION (UNII: 7IS9N8KPMG)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- ETHYLPARABEN (UNII: 14255EXE39)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- IRON (UNII: E1UOL152H7)
- CALCIUM (UNII: SY7Q814VUP)
- BARIUM (UNII: 24GP945V5T)
* 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".