NDC 11559-015 Daywear Bb Anti Oxidant Beauty Benefit Broad Spectrum Spf 35
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11559 - Estee Lauder Inc
- 11559-015 - Daywear Bb
Product Packages
NDC Code 11559-015-01
Package Description: 1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE
Product Details
What is NDC 11559-015?
What are the uses for Daywear Bb Anti Oxidant Beauty Benefit Broad Spectrum Spf 35?
Which are Daywear Bb Anti Oxidant Beauty Benefit Broad Spectrum 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)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Daywear Bb Anti Oxidant Beauty Benefit Broad Spectrum 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)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DOCOSANOL (UNII: 9G1OE216XY)
- OCTYLDODECYL STEAROYL STEARATE (UNII: 3D47Q6D93C)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS)
- POLYGONUM CUSPIDATUM ROOT (UNII: 7TRV45YZF7)
- HORDEUM VULGARE ROOT (UNII: 790S39483Z)
- FUMARIA OFFICINALIS FLOWERING TOP (UNII: VH659J61ZL)
- LEMON (UNII: 24RS0A988O)
- SACCHARINA LATISSIMA THALLUS (UNII: 68CMP2MB55)
- ROSEMARY (UNII: IJ67X351P9)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- WHEAT GERM (UNII: YR3G369F5A)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- CAFFEINE (UNII: 3G6A5W338E)
- PROPYLENE GLYCOL STEARATE (UNII: MZM1I680W0)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SUCROSE (UNII: C151H8M554)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- SQUALANE (UNII: GW89575KF9)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- UREA (UNII: 8W8T17847W)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- PROPYLENE GLYCOL LAURATES (UNII: 40KT317HGP)
- ENOXOLONE (UNII: P540XA09DR)
- TREHALOSE (UNII: B8WCK70T7I)
- FUMARIC ACID (UNII: 88XHZ13131)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- MASOPROCOL (UNII: 7BO8G1BYQU)
- XANTHAN GUM (UNII: TTV12P4NEE)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- CHROMIC OXIDE (UNII: X5Z09SU859)
- MICA (UNII: V8A1AW0880)
- FERRIC FERROCYANIDE (UNII: TLE294X33A)
- COCHINEAL (UNII: TZ8Z31B35M)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
* 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".