NDC 14783-885 Effet Parfait Rouge Amplifier Amplifying Spf 15 (salmon Essential) - Orange
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What is NDC 14783-885?
What are the uses for Effet Parfait Rouge Amplifier Amplifying Spf 15 (salmon Essential) - Orange?
Which are Effet Parfait Rouge Amplifier Amplifying Spf 15 (salmon Essential) - Orange UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Effet Parfait Rouge Amplifier Amplifying Spf 15 (salmon Essential) - Orange 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:
- DIISOPROPYL DILINOLEATE (UNII: 5323S7S2LR)
- METHYL HYDROGENATED ROSINATE (UNII: 13DHA19W9N)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- MICA (UNII: V8A1AW0880)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CANDELILLA WAX (UNII: WL0328HX19)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- ISODODECANE (UNII: A8289P68Y2)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y)
- DIPALMITOYL HYDROXYPROLINE (UNII: E6AHA53N1H)
- SHEA BUTTER (UNII: K49155WL9Y)
- .BETA.-SITOSTEROL (UNII: S347WMO6M4)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- LUFFA AEGYPTIACA SEED OIL (UNII: 1A281RJ859)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CERAMIDE 3 (UNII: 4370DF050B)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ALLANTOIN (UNII: 344S277G0Z)
- MANGANESE VIOLET (UNII: 72M48QQV8Q)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- D&C RED NO. 21 (UNII: 08744Z6JNY)
- TALC (UNII: 7SEV7J4R1U)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- STANNIC OXIDE (UNII: KM7N50LOS6)
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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".