NDC 14783-898 Effet Parfait Hydratess Long-lasting Intense Moisturizing Spf 20 (almond) - Brown
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 14783-898?
What are the uses for Effet Parfait Hydratess Long-lasting Intense Moisturizing Spf 20 (almond) - Brown?
Which are Effet Parfait Hydratess Long-lasting Intense Moisturizing Spf 20 (almond) - Brown 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)
Which are Effet Parfait Hydratess Long-lasting Intense Moisturizing Spf 20 (almond) - Brown 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:
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- DIPENTAERYTHRITYL HEXACAPRYLATE/HEXACAPRATE (UNII: 554N82UWVW)
- TRIDECYL TRIMELLITATE (UNII: FY36J270ES)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- MICA (UNII: V8A1AW0880)
- TRIDECYL STEARATE (UNII: A8OE252M6L)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- COCONUT OIL (UNII: Q9L0O73W7L)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SHEA BUTTER (UNII: K49155WL9Y)
- PALM OIL (UNII: 5QUO05548Z)
- LEVANT COTTONSEED OIL (UNII: N5CFT140R8)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- LINSEED OIL (UNII: 84XB4DV00W)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CERAMIDE 3 (UNII: 4370DF050B)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- TALC (UNII: 7SEV7J4R1U)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
* 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".