NDC 62874-005 Vitamin E Day Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 62874-005?
Which are Vitamin E Day Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Vitamin E Day 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)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- POLYESTER-10 (UNII: 212N9O2MMZ)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS)
- BARLEY (UNII: 5PWM7YLI7R)
- WHEAT GERM (UNII: YR3G369F5A)
- LAMINARIA OCHROLEUCA (UNII: 4R2124HE76)
- FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL)
- LEMON (UNII: 24RS0A988O)
- RICE BRAN (UNII: R60QEP13IC)
- ROSEMARY (UNII: IJ67X351P9)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- DOCOSANOL (UNII: 9G1OE216XY)
- GLYCERIN (UNII: PDC6A3C0OX)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- CAFFEINE (UNII: 3G6A5W338E)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- SQUALANE (UNII: GW89575KF9)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ENOXOLONE (UNII: P540XA09DR)
- TREHALOSE (UNII: B8WCK70T7I)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- MASOPROCOL (UNII: 7BO8G1BYQU)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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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".