NDC 40046-0046 Studio Moisture Fix Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 40046 - Make Up Art Cosmetics
- 40046-0046 - Studio Moisture Fix
Product Packages
NDC Code 40046-0046-1
Package Description: 1 BOTTLE in 1 CARTON / 50 mL in 1 BOTTLE (40046-0046-2)
Product Details
What is NDC 40046-0046?
Which are Studio Moisture Fix Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Studio Moisture Fix Spf 15 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- ASTROCARYUM MURUMURU SEED BUTTER (UNII: 12V64UPU6R)
- CAFFEINE (UNII: 3G6A5W338E)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- BARLEY (UNII: 5PWM7YLI7R)
- FU LING (UNII: XH37TWY5O4)
- POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- YEAST (UNII: 3NY3SM6B8U)
- WHEAT GERM (UNII: YR3G369F5A)
- SUCROSE (UNII: C151H8M554)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SQUALANE (UNII: GW89575KF9)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- STEARETH-21 (UNII: 53J3F32P58)
- POVIDONE K17 (UNII: C67P1734QJ)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CETYL ESTERS WAX (UNII: D072FFP9GU)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PROPYLENE GLYCOL DICAPRATE (UNII: U783H9JHWY)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
* 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".