NDC 40046-0039 Prep And Prime Fortified Skin Enhancer Spf 35
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 40046 - Makeup Art Cosmetics
- 40046-0039 - Prep And Prime
Product Packages
NDC Code 40046-0039-1
Package Description: 1 TUBE in 1 CARTON / 30 mL in 1 TUBE (40046-0039-2)
Product Details
What is NDC 40046-0039?
Which are Prep And Prime Fortified Skin Enhancer Spf 35 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Prep And Prime Fortified Skin Enhancer Spf 35 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DOCOSANOL (UNII: 9G1OE216XY)
- POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
- OCTYLDODECYL STEAROYL STEARATE (UNII: 3D47Q6D93C)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CAFFEINE (UNII: 3G6A5W338E)
- ENOXOLONE (UNII: P540XA09DR)
- UREA (UNII: 8W8T17847W)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SQUALANE (UNII: GW89575KF9)
- BARLEY (UNII: 5PWM7YLI7R)
- WHEAT GERM (UNII: YR3G369F5A)
- GLYCERIN (UNII: PDC6A3C0OX)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- TREHALOSE (UNII: B8WCK70T7I)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- GAMMA ORYZANOL (UNII: SST9XCL51M)
- SUCROSE (UNII: C151H8M554)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
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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".