NDC 69769-101 Soleil Forte Multi
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69769 - Linex Health & Beauty
- 69769-101 - Soleil Forte Multi
Product Packages
NDC Code 69769-101-51
Package Description: 1 TUBE in 1 BOX / 50 mL in 1 TUBE (69769-101-11)
Product Details
What is NDC 69769-101?
What are the uses for Soleil Forte Multi?
Which are Soleil Forte Multi UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Soleil Forte Multi 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- CETEARYL ISONONANOATE (UNII: P5O01U99NI)
- METHYL METHACRYLATE (UNII: 196OC77688)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- WATER (UNII: 059QF0KO0R)
- .ALPHA.,.BETA.'-DIGLYCERIN (UNII: LG6U99J4V1)
- POLYGLYCEROL POLYRICINOLEIC ACID (UNII: 3C96Y1D5T4)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GINKGO BILOBA WHOLE (UNII: 660486U6OI)
- HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- CETYL RICINOLEATE (UNII: 1P677500YD)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERYL CAPRATE (UNII: 197M6VFC1W)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- ALUMINUM STEARATES (UNII: O4D7U3B46U)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- TOCOPHEROL (UNII: R0ZB2556P8)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
- LYCIUM BARBARUM FRUIT (UNII: 930626MWDL)
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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".