NDC 45634-734 No Makeup Foundation (porcelain) Spf20
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 45634 - Nv Perricone Llc
- 45634-734 - No Makeup Foundation (porcelain) Spf20
Product Characteristics
Product Packages
NDC Code 45634-734-31
Package Description: 50.8 g in 1 BOTTLE, PUMP
Product Details
What is NDC 45634-734?
Which are No Makeup Foundation (porcelain) Spf20 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are No Makeup Foundation (porcelain) Spf20 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:
- OCTYLDODECANOL (UNII: 461N1O614Y)
- GLYCERIN (UNII: PDC6A3C0OX)
- HEPTYL UNDECYLENATE (UNII: W77QUB6GXO)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- BELLIS PERENNIS (UNII: 2HU33I03UY)
- WATER (UNII: 059QF0KO0R)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632)
- PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
- FERROUS OXIDE (UNII: G7036X8B5H)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- PEG-10 STEARATE (UNII: D3AHD468TV)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
* 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".