NDC 98132-251 Bareminerals Complexion Rescue Defense Radiant Protective Veil Broad Spectrum Spf 30 Soft Radiance
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What is NDC 98132-251?
What are the uses for Bareminerals Complexion Rescue Defense Radiant Protective Veil Broad Spectrum Spf 30 Soft Radiance?
Which are Bareminerals Complexion Rescue Defense Radiant Protective Veil Broad Spectrum Spf 30 Soft Radiance UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Bareminerals Complexion Rescue Defense Radiant Protective Veil Broad Spectrum Spf 30 Soft Radiance 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)
- PROPANEDIOL (UNII: 5965N8W85T)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- CAMELLIA JAPONICA FLOWER (UNII: KUB8101TNF)
- BUPLEURUM FALCATUM ROOT (UNII: X04E310LUY)
- UNDARIA PINNATIFIDA (UNII: ICV1OK7M1S)
- HYPERICUM ERECTUM FLOWERING TOP (UNII: IT0296HQDC)
- COCOA (UNII: D9108TZ9KG)
- LACTOBACILLUS REUTERI (UNII: 9913I24QEE)
- CERAMIDE NP (UNII: 4370DF050B)
- MANGANESE PIDOLATE (UNII: 3S6I84YKIV)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- BIOSACCHARIDE GUM-4 (UNII: 9XRL057X90)
- LEVOMENOL (UNII: 24WE03BX2T)
- ALLANTOIN (UNII: 344S277G0Z)
- PHYTOSTERYL/OCTYLDODECYL LAUROYL GLUTAMATE (UNII: 65954KGO9Q)
- LAURYL BETAINE (UNII: Y4P927Q133)
- CETYL STEARATE (UNII: 06RI5UQA7L)
- ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- DECYL ISOSTEARATE (UNII: NRB038QC02)
- POLYQUATERNIUM-51 (2-METHACRYLOYLOXYETHYL PHOSPHORYLCHOLINE/N-BUTYL METHACRYLATE; 3:7) (UNII: EL9825H96J)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- MICA (UNII: V8A1AW0880)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- SORBITAN SESQUIISOSTEARATE (UNII: VU97D01BF9)
- SODIUM METHYL STEAROYL TAURATE (UNII: JFM219LJ55)
- VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
- TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- ALCOHOL (UNII: 3K9958V90M)
- LIMONENE, (+/-)- (UNII: 9MC3I34447)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
* 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".