NDC 90069-203 Purpleu Glow Tone It Like Snow
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 90069 - Purple U Co., Ltd
- 90069-203 - Purpleu Glow Tone It Like Snow
Product Packages
NDC Code 90069-203-01
Package Description: 35 mL in 1 BOTTLE
Product Details
What is NDC 90069-203?
What are the uses for Purpleu Glow Tone It Like Snow?
Which are Purpleu Glow Tone It Like Snow UNII Codes?
The UNII codes for the active ingredients in this product are:
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
Which are Purpleu Glow Tone It Like Snow 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TROMETHAMINE (UNII: 023C2WHX2V)
- PEG-2 STEARATE (UNII: 94YQ11Y95F)
- LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HIPPOPHAE RHAMNOIDES FRUIT (UNII: AVL0R9111T)
- NYMPHAEA ALBA FLOWER (UNII: 40KQ7Q535O)
- PRUNUS SERRULATA FLOWER (UNII: 60I4615G0K)
- 4-(P-HYDROXYPHENYL)-2-BUTANONE (UNII: 7QY1MH15BG)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- PEG-100 STEARATE (UNII: YD01N1999R)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- TRICETEARETH-4 PHOSPHATE (UNII: 69534Y66NO)
- JOJOBA OIL (UNII: 724GKU717M)
- PROPANEDIOL (UNII: 5965N8W85T)
- ETHYLENE GLYCOL MONOBENZYL ETHER (UNII: 06S8147L47)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ROSA DAMASCENA FLOWER OIL (UNII: 18920M3T13)
- NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
- GLUTATHIONE (UNII: GAN16C9B8O)
- HYDROLYZED GLYCOSAMINOGLYCANS (BOVINE; 50000 MW) (UNII: 997385V0VV)
- CERAMIDE NP (UNII: 4370DF050B)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- OCTANEDIOL (UNII: 806K32R50Z)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- OCTISALATE (UNII: 4X49Y0596W)
- MICA (UNII: V8A1AW0880)
- ADANSONIA DIGITATA FRUIT (UNII: 51N9TR1W6P)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- HYALURONIC ACID (UNII: S270N0TRQY)
* 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".