NDC 68828-049 Jafra Pro Face Lift Spf 20
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68828 - Jafra Cosmetics International
- 68828-049 - Jafra Pro Face Lift
Product Packages
NDC Code 68828-049-11
Package Description: 1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE (68828-049-67)
Product Details
What is NDC 68828-049?
What are the uses for Jafra Pro Face Lift Spf 20?
Which are Jafra Pro Face Lift Spf 20 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Jafra Pro Face Lift Spf 20 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:
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
- N-ACETYL DIPEPTIDE-1 (UNII: HA41Z1UF8D)
- CETYL ESTERS WAX (UNII: D072FFP9GU)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- COCO GLUCOSIDE (UNII: ICS790225B)
- MACROCYSTIS PYRIFERA (UNII: K31S3OG5C4)
- PULLULAN (UNII: 8ZQ0AYU1TT)
- NIACINAMIDE (UNII: 25X51I8RD4)
- SOY PROTEIN (UNII: R44IWB3RN5)
- CORN (UNII: 0N8672707O)
- XANTHAN GUM (UNII: TTV12P4NEE)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- TREHALOSE (UNII: B8WCK70T7I)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- POLIDRONIUM CHLORIDE (UNII: 6716Z5YR3G)
- UREA (UNII: 8W8T17847W)
- GLYCERIN (UNII: PDC6A3C0OX)
- OAT (UNII: Z6J799EAJK)
- COCONUT OIL (UNII: Q9L0O73W7L)
- CUCUMBER JUICE (UNII: 61845009SP)
- SANDALWOOD (UNII: 3641YW25N2)
- ROSA DAMASCENA FLOWER OIL (UNII: 18920M3T13)
- APPLE JUICE (UNII: 9871T0PD5P)
- PASSIFLORA INCARNATA FRUIT (UNII: SF206I8G4P)
- APRICOT JUICE (UNII: YX3B7ZG375)
- RASPBERRY JUICE (UNII: 427AYI9PDE)
- CANANGA ODORATA FLOWER (UNII: 76GTF6Z97M)
- MUSKMELON (UNII: ZV095H5633)
- C20-22 ALKYL PHOSPHATE (UNII: L4VKP0Y7RP)
- C20-22 ALCOHOLS (UNII: O4M0347C6A)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ALARIA ESCULENTA (UNII: EJ9JK8J58D)
- YEAST (UNII: 3NY3SM6B8U)
- TRICALCIUM PHOSPHATE (UNII: K4C08XP666)
- MORINDA CITRIFOLIA LEAF (UNII: 7UOL7P5FF5)
- PAPAYA JUICE (UNII: AZ5XLY17KM)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- PICHIA JADINII (UNII: 8JRL032K80)
- BETA VULGARIS POLLEN (UNII: W7NU4B5CIY)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- LAUROYL LYSINE (UNII: 113171Q70B)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- SOYBEAN OIL (UNII: 241ATL177A)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- TOCOPHEROL (UNII: R0ZB2556P8)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- PANTHENOL (UNII: WV9CM0O67Z)
- TROLAMINE (UNII: 9O3K93S3TK)
- EDETATE TRISODIUM (UNII: 420IP921MB)
- PEG-4 LAURATE (UNII: AYF4VM3N1Z)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
- BENZYLIDENE DIMETHOXYDIMETHYLINDANONE (UNII: 75HIF3C97L)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- WATER (UNII: 059QF0KO0R)
* 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".