NDC 40046-0033 Studio Moisture Tint Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 40046-0033?
Which are Studio Moisture Tint Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Studio Moisture Tint 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- STEARETH-21 (UNII: 53J3F32P58)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- TROMETHAMINE (UNII: 023C2WHX2V)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CAFFEINE (UNII: 3G6A5W338E)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- SUCROSE (UNII: C151H8M554)
- SORBITOL (UNII: 506T60A25R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TREHALOSE (UNII: B8WCK70T7I)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- STEARETH-2 (UNII: V56DFE46J5)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
* 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".