NDC 67938-0802 Ceramide Lift And Firm Day Broad Spectrum Sunscreen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 67938-0802?
What are the uses for Ceramide Lift And Firm Day Broad Spectrum Sunscreen Spf 30?
Which are Ceramide Lift And Firm Day Broad Spectrum Sunscreen Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Ceramide Lift And Firm Day Broad Spectrum Sunscreen Spf 30 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCOA BUTTER (UNII: 512OYT1CRR)
- SHEA BUTTER (UNII: K49155WL9Y)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- CERAMIDE 1 (UNII: 5THT33P7X7)
- CERAMIDE 3 (UNII: 4370DF050B)
- CERAMIDE 6 II (UNII: F1X8L2B00J)
- ALPINIA ZERUMBET LEAF (UNII: MS8P33AMKX)
- ABELMOSCHUS MOSCHATUS SEED (UNII: UN2QZ55I88)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- RETINYL LINOLEATE (UNII: 61911N8D6W)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- TOCOPHEROL (UNII: R0ZB2556P8)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- TREHALOSE (UNII: B8WCK70T7I)
- UREA (UNII: 8W8T17847W)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- OMEGA-3 FATTY ACIDS (UNII: 71M78END5S)
- PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
- SUCROSE (UNII: C151H8M554)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- PEG-8 LAURATE (UNII: 762O8IWA10)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- BENZYL BENZOATE (UNII: N863NB338G)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- CITRAL (UNII: T7EU0O9VPP)
- EUGENOL (UNII: 3T8H1794QW)
- GERANIOL (UNII: L837108USY)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SORBIC ACID (UNII: X045WJ989B)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
* 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".